Loss of Tmem30a leads to photoreceptor degeneration

Zhang, Lin; Yang, Yeming; Li, Shujin; Zhang, Shanshan; Zhu, Xiong; Tai, Zhengfu; Yang, Mu; Liu, Yuqing; Guo, Xinzheng; Chen, Bo; Jiang, Zhilin; Lu, Fang; Zhu, Xianjun

doi:10.1038/s41598-017-09506-5

Download PDF

Article
Open access
Published: 24 August 2017

Loss of Tmem30a leads to photoreceptor degeneration

Lin Zhang^1,2^na1,
Yeming Yang^1,2^na1,
Shujin Li^1,4,
Shanshan Zhang¹,
Xiong Zhu¹,
Zhengfu Tai^1,4,
Mu Yang^1,4,
Yuqing Liu^1,2,
Xinzheng Guo⁵,
Bo Chen⁵,
Zhilin Jiang¹,
Fang Lu^1,2 &
…
Xianjun Zhu^1,2,3,4

Scientific Reports volume 7, Article number: 9296 (2017) Cite this article

2749 Accesses
17 Citations
1 Altmetric
Metrics details

Subjects

Abstract

Phosphatidylserine (PS) is asymmetrically distributed between the outer and inner leaflets of the plasma membrane in eukaryotic cells. PS asymmetry on the plasma membrane depends on the activities of P4-ATPases, and disruption of PS distribution can lead to various disease conditions. Folding and transporting of P4-ATPases to their cellular destination requires the β subunit TMEM30A proteins. However, the in vivo functions of Tmem30a remain unknown. To this end, we generated retinal-specific Tmem30a-knockout mice to investigate its roles in vivo for the first time. Our data demonstrated that loss of Tmem30a in mouse cone cells leads to mislocalization of cone opsin, loss of photopic electroretinogram (ERG) responses and loss of cone cells. Mechanistically, Tmem30a-mutant mouse embryonic fibroblasts (MEFs) exhibited diminished PS flippase activity and increased exposure of PS on the cell surface. The broad loss of Tmem30a in adult mice led to a reduced scotopic photoresponse, mislocalization of ATP8A2 to the inner segment and cell body, and increased apoptosis in the retina. Our data demonstrated novel essential roles of Tmem30a in the retina.

Spata7 is required for maintenance of the retinal connecting cilium

Article Open access 02 April 2022

Jiaxiong Lu, Kaitlyn Xiong, … Rui Chen

Mdm1 ablation results in retinal degeneration by specific intraflagellar transport defects of photoreceptor cells

Article Open access 28 September 2022

Youlim Son, Soo-Jin Kim, … Jae-Ryong Kim

ER complex proteins are required for rhodopsin biosynthesis and photoreceptor survival in Drosophila and mice

Article Open access 01 July 2019

Liangyao Xiong, Lin Zhang, … Tao Wang

Introduction

Phospholipids are asymmetrically distributed between the outer and inner leaflets of the plasma membrane in eukaryotes^{1, 2}. Phosphatidylserine (PS) is primarily located in the inner cytoplasmic leaflet. PS flippases, which belong to the P4-ATPase family, transport aminophospholipids from the exoplasmic to the cytoplasmic leaflet of cell membranes by utilizing ATP^3,4,5,6. Aminophospholipid asymmetry in the cellular membrane that is maintained by P4-ATPases is critical for various biological processes, such as blood coagulation regulation⁷, vesicular protein transport⁸, the recognition of apoptotic cells⁹ and sperm capacitation¹⁰.

The fact that mutations in several P4-ATPases, including ATP8B1, ATP8A2 and ATP11C, lead to various human diseases highlights the importance of P4-ATPases^{11,12,13,14,15,16}. For instance, mutations in ATP8B1 cause progressive familial intrahepatic cholestasis type I and benign recurrent intrahepatic cholestasis¹¹, and mutations in ATP8A2 cause axonal degeneration in mice and a severe neurological disorder that is characterized by cerebellar ataxia, mental retardation and disequilibrium syndrome^{12, 14,15,16}. Mice deficient in Atp8a1 display increased externalization of PS on the plasma membranes of hippocampal cells and a deficiency in hippocampus-dependent learning¹³. In addition, Atp10c is associated with Angelman syndrome¹⁷, and Atp11c-deficient mice have recently been reported to exhibit B-cell lymphopenia, anaemia and intrahepatic cholestasis^18,19,20,21. During apoptosis, ATP11C is also inactivated by caspases²².

P4-ATPases, except ATP9A and ATP9B, are associated with members of the conserved CDC50 protein family²³. There are three CDC50 genes in the mammalian genome (CDC50A, CDC50B and CDC50C, also named TMEM30A, TMEM30B and TMEM30C, respectively), which encode N-glycosylated proteins with two transmembrane segments²³. Emerging evidence indicates that TMEM30 proteins are essential for the folding and exporting of P4-ATPases from the endoplasmic reticulum^{24,25,26,27,28,29}. TMEM30 proteins also play roles in the catalytic reaction cycle of P4-ATPase^{23, 29}. Akin to the beta subunit of the Na+/K+ ATPase, TMEM30 proteins act as the beta-subunit of P4-ATPase and participate in ATP-dependent phospholipid transport^{23, 29, 30}. In the retina, TMEM30A was expressed in photoreceptor cells and is critical for the stable expression, transport and lipid transport activity of the P4-ATPase ATP8A2, as determined by heterologous expression studies and in vitro analysis³¹. In the retina, Atp8a2 is expressed in photoreceptor cell and essential for retinal photoreceptor function and survival³². Loss of ATP8A2 in either Atp8a2 mutant wl or vmd, or knockout mouse model led to reduced scotopic and photopic ERG responses, shorted outer segment, thinner outer nuclear layer and degeneration of rod cells³². However, the in vivo functions of Tmem30a in the mammalian retina are yet to be elucidated.

In this study, we generated the first retina-specific Tmem30a-knockout mice and investigated the in vivo functions of Tmem30a in mice. Our data showed that loss of Tmem30a in mouse cone cells led to the mislocalization of cone opsin protein, the loss of photopic electroretinogram (ERG) responses and the loss of cone cells. Broad deficiency of Tmem30a in adult mice causes a reduced scotopic photoresponse and the mislocalization of PS flippase ATP8A2 to the inner segment and cell body, which leads to the dysfunction and death of rod cells. The loss of Tmem30a in mouse embryonic fibroblasts (MEFs) resulted in reduced PS flippase activity and increased exposure of PS on the cell surface. Collectively, our data demonstrated that the loss of Tmem30a leads to mislocalization of PS flippase ATP8A2 and degeneration of retinal rod and cone cells. Thus, our studies highlight an essential role for Tmem30a in the retina.

Results

Tmem30a is essential for survival

Tmem30a is broadly expressed in the retina, brain, cerebellum, liver, heart, kidney, spine and testis (Figure S1). To investigate the role of Tmem30a in vivo, we generated Tmem30a-knockout mice (Fig. 1). In the modified Tmem30a allele, an FRT-flanked bacterial beta-Gal reporter gene with an upstream splicing acceptor and a neomycin expression cassette were inserted into intron 2–3. Exon 3 was flanked by two loxP sites (Fig. 1A). This constitutes a knockout allele with the potential to be converted into a conditional knockout allele. With a splicing acceptance site (SA) in place in intron 2–3, transcription of Tmem30a mRNA is disrupted, resulting in a null allele (Tmem30a ^tm1Xjz). The knockout allele was confirmed by long range PCR: a 6.3-Kb fragment was amplified for the 5′arm and a 6.6-Kb fragment was amplified for the 3′arm (Figure S2). PCR genotyping was used to identify possible homozygous knockout mice from their wild-type and heterozygous littermates (Fig. 1B). Of 64 pups tested on P1, no homozygous mutant mice were observed (Table S1). Therefore, Tmem30a is essential for early embryonic development.

The role of Tmem30a in the retina

In the retina, TMEM30A localized to the outer segment and inner segment (with weak expression) of photoreceptor cells, similar to ATP8A2^{31, 32} (Fig. 1D). The specificity of mouse monoclonal anti-TMEM30A antibody was verified (Figure S1B, C). To study the role of Tmem30a after early development, the Tmem30a knockout first allele was crossed to Flper mice³³ to remove the FRT-flanked LacZ reporter and Neo cassette and to generate a conditional allele, Tmem30a ^tm1.1Xjz. For simplicity, this allele is referred to as Tmem30a ^loxp (Fig. 1C). Pan-neural deletion of Tmem30a using Nestin-Cre³⁴ led to early lethality (Table S2). To investigate the role of Tmem30a in the retina, we generated retinal neural deletion mutant mice using Six3-Cre³⁵ (Figure S3A). Tmem30a expression was diminished to 25% in mutant retina (Figure S3A). Loss of Tmem30a in retinal neuronal progenitor cells resulted in the massive loss of neural cells and the degeneration of retina layers at P12 (Figure S3B). At two months of age, no retina tissue was left in the mutant retina (Figure S3C).

Loss of Tmem30a in cone cells leads to cone-photoreceptor defects

To investigate the role of Tmem30a in photoreceptor cells, we generated a cone-photoreceptor knockout line using human red/green pigment gene promoter (HRGP-Cre) mice³⁶. In the HRGP-Cre mouse, Cre expression is initiated on postnatal day 7–10 and is specific for M-opsin-expressing cone cells²⁰. Mice homozygous for the Tmem30a floxed allele (Tmem30a ^loxp/loxp) were mated to HRGP-Cre (cone-Cre), Tmem30a ^loxp/+ mice to generate Tmem30a ^loxp/loxp HRGP-Cre (mutant) and Tmem30a ^loxp/+ HRGP-Cre (control) mice. Cre-positive controls were used in the analysis to ensure that any phenotypic difference between mutants and controls was due to the loss of Tmem30a. The rd1 mutation in the original HRGP-Cre mice was screened out by mating them to C57BL/6J mice before the experiment. We verified the specificity of HGRP-Cre using a TdTomato reporter. To do this, we crossed ROSA26-TdTomato reporter mice to Tmem30a ^loxp/loxp HRGP-Cre mice to generate Tmem30a ^loxp/loxp HRGP-Cre Rosa-TdTomato mice. In the presence of the Cre enzyme, the stop codon before the TdTomato expression cassette was removed, and Rosa was expressed in Cre-positive cells (Fig. 2A). In Cre-expressing cells, M-opsin expression was greatly diminished (Fig. 2A), suggesting that Tmem30a function is important for M-opsin expression and stability. Photopic ERG analysis revealed diminished ERG responses in the cone mutant retina (Fig. 2B,C). No recognized a-wave or b-wave was observed in cone-knockout mice.

Close examination of P16 cross-section retinas in higher-magnification images revealed mislocalization of M-opsin to the inner segment (IS) and to the cell bodies, while there was no obvious loss of cone cells (arrows, Fig. 3A,B). No protein expression can be observed for GRK1 and CNG3, two proteins expressed in cones (Figs S6 and 7). No mislocalized GRK1 or CNG3 was observed in the cell body, probably due to rapid degradation of these proteins in mutant cones. After P16, the number of cone cells in the mutants declined quickly, such that very little cone opsin staining could be seen in the cone outer segment at P42 (Figure S4A). We next analysed the number of cone cells in the mutant mice by immunostaining whole-mount retinas with M-opsin. This whole-mount study enabled us to survey cones across the whole retina and to avoid possible artefacts introduced by examining sections from different places in the retina. At P16, approximately equal numbers of cone outer segments were found in the mutant and the control mice (Fig. 3C). At P42, no cone cells were observed (Figure S4B4). In the P42 vmd mutant retina, there were similar numbers of cone cells to those in controls (Figure S5). However, close examination of the cross-section of retinas in higher-magnification images revealed a reduced amount of opsin in the cone OS and showed that the OS did not develop properly (Figure S5). Apparently, loss of Tmem30a in cone cells leads to a more severe phenotype than the loss of Atp8a2 in vmd mice (Figs S4 and 5). Because TMEM30A binds to multiple PS flippases^{20, 24}, including ATP8A2, these data suggest that other PS flippase(s) may play a role in the retina.

Deletion of Tmem30a in adult animals leads to rod cell degeneration

To confirm our finding with M-opsin-Cre and to assess the role of Tmem30a in developed photoreceptor cells, we used tamoxifen-activated CAG-CreER³⁷ to remove Tmem30a in adult mice. In CAG-CreER animals, Cre is broadly expressed under the control of a chicken beta actin promoter coupled with a cytomegalovirus (CMV) immediate-early enhancer promoter. The Cre recombinase is fused to a mutant form of the mouse oestrogen receptor ligand-binding domain, which does not bind natural ligand at physiological concentrations but will bind the synthetic ligand, 4-hydroxytamoxifen. Upon induction with tamoxifen, CAG-CreER induces the deletion of loxP-flanked exon 3 in all cells of the retina. We treated P20 animals with tamoxifen and assessed the retina at P25, P27 and P30. Upon induction, Tmem30a was efficiently deleted in the retina. We utilized ERG analysis to assess physiological status of the retina. At P25, no visible difference was observed in the mutant retina (Fig. 4A). However, at P27, ERG test revealed reduced amplitudes for both a waves and b waves (Fig. 4B). The amplitude of a wave in the mutant retina was reduced to 50% of that of controls (Fig. 4B3). The amplitude of b wave in the mutant retina was reduced to 40% of that of controls (Fig. 4B4).

We examined tissue sections stained with haematoxylin and eosin (H&E) to assess the structures of mutant retinas at P25, P27 and P30. At P25 no obvious difference was observed between the mutant and the control mice (Fig. 5A,B,C). However, at P27, a shorter outer segment and a thinner outer nuclear layer (ONL) were seen in the mutant retina (Fig. 5D,E,F). The mutant ONL was reduced to approximately 50% of the control (Fig. 5F). There were also few cells in the retina ganglion cell layer. At P30, no OS was left, and the ONL was reduced to 2–3 cells per row in the mutant retina, compared with 10–11 cells per row in the control retina (Fig. 5G,H,I). To investigate the molecular mechanisms underlying these severe phenotypes, we examined retina sections by immunohistochemistry using various antibodies. At P25 and P27, no TMEM30A staining wad observed in the photoreceptor layer in mutant retina, confirming loss of TMEM30A (Fig. 6A). At P25, the expression level of TMEM30A in mutant retina was reduced to 21% of that of controls (Fig. 6B). ATP8A2, the P4-ATPase expressed in the retina, requires its beta subunit TMEM30A for subcellular localization. To assess the effect of Tmem30a deficiency on ATP8A2 in the retina, we examined expression and localization of ATP8A2 in Tmem30a mutant retina. At P25, the expression level of ATP8A2 was reduced to 79% of that of controls, while at P27 ATP8A2 expression level in the mutant retina was reduced to 57% of that of controls (Fig. 6C). Immunostaning revealed that ATP8A2 was mislocalized to the inner segment and cell bodies in the mutant retina (Fig. 6D).

PS exposure on the cell surface acts as an “eat-me signal” to mark apoptotic cells for macrophage clearance^{22, 38}. The loss of PS asymmetry in the Tmem30a-mutant retina prompted us to examine the apoptotic signalling pathway in the mutant retina. At P25, compared with the control retina, TUNEL staining increased in the mutant retina (Fig. 7A,B), and at P27, more positive staining cells were observed (Fig. 7A,B). Cleaved caspase 3, an important molecule for cell apoptosis, was up-regulated in P25 and P27 retina (Fig. 7C,D). These data indicated that the loss of TMEM30A activity in the retina led to the initiation of the cell apoptosis pathway, which explains the rapid loss of photoreceptor cells in mutant retina.

Loss of PS flippase activity and PS asymmetry in mutant MEF cells

To investigate the cellular pathways in Tmem30a knockout cells, we generated MEFs using Tmem30a ^loxp/loxp CAG-CreER and Tmem30a ^loxp/loxp embryos. The addition of tamoxifen to the culture medium could effectively remove the loxp-flanked exon 3, generating mutant MEFs. TMEM30A expression in mutant MEFs was reduced to 20% of control cells (Fig. 8A). Mutant MEFs grew normally, and no apparent morphological abnormalities could be observed. However, annexin V staining revealed a loss of PS asymmetry and more exposure of PS on the outer membrane in mutant MEFs (Fig. 8B,C). In agreement with this finding, loss of Tmem30a led to decreased fluorescence NBD-PS uptake. PS flippase activity in mutant cells was reduced to 30% of control cells (Fig. 8D–F). Compared to wildtype cells, the expression levels of Atp8a2, Atp8b4 and Atp11a, Atp11c were reduced in mutant MEFs (Figure S8). These data demonstrated that loss of Tmem30a resulted in reduced PS flippase activity in the cell.

Discussion

In this study, we analysed the role of Tmem30a in the retina by generating novel retina-specific knockout mice. Tmem30a-knockout mice were embryonic lethal, revealing the importance of this gene in vivo (Table S1). The pan-neuronal knockout of Tmem30a using Nestin-Cre also led to embryonic lethality (Table S2). Therefore, Tmem30a-knockout mice exhibit more severe phenotypes than the five available PS flippase-knockout mice, including Atp8b3, Atp8b1, Atp8a2, Atp8a1 and Atp11c. This finding is in agreement with previous reports showing that TMEM30A binds to multiple P4-ATPases^{23, 26}.

Tmem30a deficiency in the cone cells led to diminished photopic ERG responses and the rapid degeneration of cone cells (Figs 2–3, S4). At P16, opsin accumulated in the cone cell bodies (Fig. 3A) and lead to the death of affected cells. At P16, there were similar numbers of M-opsin-positive cells in the mutant retina and the controls (Fig. 2C). However, the cone OS appeared shorter, and by P42, no cone cells were left (Figure S4). By contrast, in vmd mice, no apparent accumulation of opsin in the IS and cell body could be seen at P42, although the opsin-positive OS was shorter (Figure S5). Apparently, the loss of Tmem30a in cone cells resulted in more severe phenotypes than the loss of Atp8a2, which is likely due to the fact that TMEM30A binds multiple P4-ATPases in the retina.

In Tmem30a-mutant rod cells, ATP8A2 expression was reduced and ATP8A2 mislocalized to the IS and cell bodies (Fig. 6C,D), and these data are consistent with previous reports that used a Tmem30a-knockout cell line. Segawa et al. showed that the loss of ATP11C in the human KBM7 cell line resulted in reduced PS flippase activity²². Moreover, the internalization of NBD-PS was completely defective in Tmem30a-mutant cells, and Tmem30a-mutant cells exposed PS on the cell surface²². Indeed, in Tmem30a-deficient MEFs, the loss of Tmem30a leads to decreases in PS flippase activity and exposure of PS on the outer leaflet, as revealed by annexin V staining (Fig. 8). In the retina, the loss of Tmem30a resulted in rod cell apoptosis (Fig. 7). The rapid degeneration of rod cells was likely to be mediated through the apoptotic pathway.

Mutations in Atp8a2 in mice have been shown to cause axonal degeneration and the degeneration of both rod and cone cells in the retina¹⁶. In addition, disruption of ATP8A2 leads to severe neurological disorders that are characterized by cerebellar ataxia, mental retardation and disequilibrium syndrome in humans. A missense mutation (NM_016529 c.1128C > G, p.I376M) was identified in three patients from a consanguineous family in Turkey¹⁵, and these patients exhibited encephalopathy, cerebellar atrophy, body tremor and mental retardation. These patients were able to sit with no support and crawl on their hands and feet, although no ophthalmology evaluation was performed on these patients due to the lack of consent. Very recently, two unrelated patients were reported to exhibit encephalopathy, mental retardation, severe hypotonia, a normal retina and optic atrophy¹⁴. The mutations that were uncovered included a homozygous mutation of ATP8A2, c.1287G > T, p.K429N, and the compound heterozygous mutations c.1630G > C, p.A544P and c.1873C > T, p.R625W, emphasizing the importance of PS flippases in the central nervous system¹⁴. Based on our mouse data, homozygous mutations that affect the function of Tmem30a are likely to be embryonic lethal. Given the finding that Tmem30a is broadly expressed in various tissues (Figure S1) and binds to multiple P4-ATPases, its roles in different tissues warrant further investigation.

Collectively, our data demonstrate novel roles for Tmem30a in retinal photoreceptor cells. Tmem30a deficiency resulted in a diminished photopic ERG response and in the accumulation of opsin in the inner segment and in cell bodies in cone cells. The deletion of Tmem30a also resulted in a loss of PS flippase activity and the exposure of PS on the cell surface in MEFs. Together, our studies highlight the importance of Tmem30a in the retina.

Methods

Experimental animals and genotyping

All animal study protocols were approved by the Animal Care and Use Committee of the Hospital of the University of Electronic Science and Technology and Sichuan Provincial People’s Hospital. All experimental procedures and methods were carried out in accordance with the approved study protocols and relevant regulations. Mice were raised in cyclic lighting conditions with a 12-hour light and 12-hour dark cycle.

The Tmem30a-knockout first targeting vector was obtained from the Knockout Mouse Project (KOMP) Repository. The targeting vector was linearized by AscI and transfected by electroporation of 129/SvEv embryonic stem cells. Homologously recombined positive clones were selected by neomycin, screened by PCR and confirmed by long-range PCR at both the 5′ and the 3′ arms. The primers used for long-range PCR for the 5′ arm were as follows: Tmem30a-GF3, GAGGAAGCGGAAGTGTAAGTTACCAAG; and Tmem30a-LAR3, CACAACGGGTTCTTCTGTTAGTCC. The primers used for long-range PCR for the 3′ arm were as follows: Tmem30a-GR3, GTGTGAAGTCAACGTCATTATCGGAGAATC; and Tmem30a-RAF5, CACACCTCCCCCTGAACCTGAAAC. Two independent clones of the targeted stem cells were microinjected into C57BL/6 J blastocysts. Resulting chimaera male mice were mated to C57BL/6 J female mice to generate F1 heterozygous founders. Heterozygous F1 (designated as Tmem30a ^tm1Xjz) mice were crossed to generate F2 offspring. To generate a conditional allele of Tmem30a, heterozygous F1 mice were crossed to Flper mice³³ (strain name: B6.129S4-Gt(ROSA)26Sortm1(FLP1)Dym/RainJ, stock number 009086, also named ROSA26::FLPe knock in, https://www.jax.org/strain/009086) to remove the FRT-flanked LacZ reporter and neomycin cassette. The resulting conditional allele of Tmem30a was designated as Tmem30a ^tm1.1Xjz. Tmem30a ^tm1.1Xjz mice (for simplicity, designated as Tmem30a ^loxp) were backcrossed to C57BL/6 J mice for 5 generations.

Tmem30a ^loxp/+ mice were mated to Nestin-Cre³⁴ mice to generate Tmem30a ^loxp/+ Nestin-Cre mice. Tmem30a ^loxp/+ Nestin-Cre mice were crossed to Tmem30a ^loxp/loxp homozygous mice to generate a pan-neuronal deletion of Tmem30a. Tmem30a ^loxp Six3-Cre mice were generated by crossing Tmem30a ^loxp/+ mice to the Six3-Cre line³⁵. Cone-specific knockout mice were generated by crossing Tmem30a ^loxp/+ to HRGP-Cre mice³⁶. The rd1 mutation was bred out before the experiment. Tmem30a ^flox/+mice were crossed to the broadly expressed inducible CRE CAG-Cre-ER mice³⁷ (stock Tg(CAG-cre/Esr1*) 5Amc/J, https://www.jax.org/strain/004453) to generate inducible adult knockout mice. To monitor the efficiency of Cre-mediated deletion of the floxed exon, a TdTomato reporter was used (strain name: B6.Cg-Gt(ROSA)26Sortm14(CAG-TdTomato)Hze/J, also named Ai14D, http://jaxmice.jax.org/strain/007914.html)³⁸. The reporter contains a loxP-flanked STOP cassette that prevents transcription of the downstream CAG promoter-driven red fluorescent protein variant TdTomato. In the presence of Cre recombinase, the reporter mice will have the STOP cassette removed in the Cre-expressing tissue(s) and will express TdTomato. Because this CAG promoter-driven reporter construct was inserted into the Gt(ROSA)26Sor locus, TdTomato expression was determined by the tissue(s) that expressed Cre recombinase.

The Atp8a2 mutant vmd strain was purchased from The Jackson Laboratory and was described in Zhu et al.¹⁶. vmd is a 9167 bp genomic deletion that results in removal of the entire exon 32 of Atp8a2. This results in a 32 amino acid deletion in the ninth transmembrane domain of ATP8A2 and disrupted the function of ATP8A2¹⁶. This allele was backcrossed to C57BL/6 J for 10 generation to remove rd1 mutation in the original C3H background and generated congenic strain of vmd on C57BL/6 J. As standard practice for vmd-mutant mice, dry food was supplemented with a soft maintenance diet (DietGel 76 A, Clear H₂O, Portland, ME, USA).

Tamoxifen treatment

A total of 100 mg of tamoxifen salt (Sigma, St Louis, MO, USA) was dissolved in 10 ml of ethanol as a stock solution. On the day of injection, a 1 mg/ml working solution was prepared by mixing 10 mg/ml stock solution with corn oil (Sigma, Sigma, St Louis, MO, USA) and mixed well. On P20, mutant and control mice were intraperitoneally injected with a daily dosage of 25 mg/Kg body weight for three days.

Genotyping by PCR

Genomic DNA extracted from mouse-tails was amplified by PCR using primers for the Tmem30a gene (Tmem30a-Loxp2-F, 5′-attccccttcaagatagctac -3 and Tmem30a-Loxp2-R, 5-aatgatcaactgtaattcccc -3). Amplification was performed using a master mix (Invitrogen, USA). The first cycle consisted of 95 °C for 2 minutes, followed by 33 cycles of 94 °C for 15 seconds, 58 °C for 20 seconds and 72 °C for 30 seconds. Cre was genotyped using generic Cre primers: Cre-F, TGCCACGACCAAGTGACAGCAATG, and Cre-R, ACCAGAGACGCAAATCCATCGCTC). TdTomato mice were genotyped using the following protocol provided by the JAX mouse service: oIMR9020, 5′-AAGGGAGCTGCA GTGGAGTA-3′; oIMR9021, 5′-CCGAAAATCTGTGGGAAGTC-3′; oIMR9103, 5′--GGCATTAAAGCAGCGTATCC-3′; and oIMR9105, 5′-CTGTTCCTGTACGGCATGG-3′. FLPer mice were genotyped using the following primers: oIMR1348, 5′-CAC TGATATTGTAAGTAGTTT gC-3′; oIMR1349, 5′-CTA GTGCGAAGTAGT GATCAGG-3′; oIMR1427, 5′-TGTTTTGGAGGCAGGAAGCACTTG-3′; and oIMR1428, 5′-AAATACTCCGAGCGGATCACAAG-3′.

For the vmd genomic deletion, three primers flanking the region were used to distinguish between the wild-type and mutant alleles: vmdF, 5′-CTAACTGTGGCTCACTTACCTCCT-3′; vmdR1, 5′-TCCTCCAGAACATTGAAGTGACTA-3′; and vmdR2, 5′-TGCATCTTGATTTTTGCTTTGTAT-3′. A 403-bp amplicon was produced in the presence of the wild-type allele using the vmdF and vmdR1 primers, and a 207-bp amplicon was produced in the presence of the mutant vmd allele using the vmdF and vmdR2 primers.

RT-PCR

Tissues from 1- to 2-month-old animals were dissected and placed into RNAlater (Ambion, Austin, TX, USA) at room temperature. Total RNA was prepared from these tissues using TRIzol reagent (Life Technologies) according to the manufacturer’s instructions. RNA samples were treated with RNase-free DNaseI (Ambion, Austin, TX, USA) to remove genomic DNA, and the RNA concentration was determined with a NanoDrop (ND-1000) spectrophotometer. A total of 3 µg of RNA was reverse transcribed using random primers and the MessageSensor RT kit (Ambion, TX, USA). The primers used for RT-PCR for mouse gene studies were listed in the material and method section of supplementary data. PCR was performed with Taq polymerase (New England Biolabs, MA, USA), and the PCR products were resolved on 3% agarose gels.

Histology and measurement of outer nuclear layer

For haematoxylin and eosin staining (H&E), eyes from WT and knockout (KO) mice were removed, marked on the nasal side for orientation and fixed overnight in 1.22% glutaraldehyde and 0.8% paraformaldehyde in 0.08 M phosphate buffer, embedded in paraffin, and cut into 5-µm sections. H&E stained sections were used to count the rows of photoreceptors in the outer nuclear layer³⁶. Three measurement of the outer nuclear layer were taken every 200 μm from the optic nerve and averaged. The optic nerve was designated as 0 µm.

Electroretinograms

Control and mutant mice were dark-adapted overnight, and all subsequent procedures were performed under dim red light. Animals were anesthetized with a combination of ketamine (16 mg/kg body weight) and xylazine (80 mg/kg body weight) in normal saline. Dark-adapted ERGs were recorded on with the responses to short-wavelength flashes over 4.0 log units to the maximum intensity with the Espion Visual Electrophysiology System from Diagnosis, LLC (Littleton, MA, USA). Cone-mediated ERGs were recorded with white flashes after 20 min of complete light adaptation.

Immunohistochemistry

For immunohistochemistry, enucleated eyes were removed, marked at the nasal side for orientation and fixed for 1 hour in 4% paraformaldehyde in 100 mM phosphate buffer (PB) (pH 7.4) and then cryoprotected in 30% sucrose. Tissues were embedded in optimal cutting temperature solution (OCT) and frozen on dry ice for sectioning. Sections were blocked and permeabilized with 10% normal goat serum and 0.2% Triton X-100 in phosphate buffer for 30 minutes. Labelling with various antibodies was performed as previously described¹⁶. Mouse monoclonal against cleaved caspase 3 was purchased from R&D Systems (Minneapolis, MN, USA). Primary antibodies were diluted in phosphate buffer containing 5% normal goat serum and 0.1% Triton X-100 at the following concentrations: ATP8A2 polyclonal antibody (purified 0.3 µg/ml), TMEM30A monoclonal antibody (Cdc50-7F4), PMC 1D1 monoclonal antibody to the CNGA1 channel subunit, Rho1D4 monoclonal antibody to rhodopsin were gifts from Dr. Robert Molday, University of British Columbia, Canada. GRK1 antibody, Alex-Fluor-594-labelled annexin V (Invitrogen, Shanghai, China). Sections were incubated with primary antibodies overnight. Then, the sections were washed with PB three times and labelled for 1 hour with Alexa-Fluor-488- or Alexa-Fluor-594-labelled goat anti-mouse or anti-rabbit Ig secondary antibody (diluted 1:500) and counterstained with DAPI.

Quantification of mislocalized M-Opsin in the cell bodies of cones was performed as following: P16 cross-section retinas were staining with M-Opsin opsin (AB5405, AB5407; Millipore, MA, USA) and DAPI and higher-magnification images were captured on a Leica SP8 confocal microscope. The number of cones with mislocalized M-Opsin to the inner segment (IS) and to the cell bodies was counted on 100 µm ONL segment at the dorsal side 500 µm to the optic nerve.

Retinal whole mounts were prepared as previously described¹⁶. Mouse eyes were lightly fixed for 1 hour after light onset with 4% paraformaldehyde for 15 minutes. The retina was dissected from the retinal pigment epithelial layer and fixed for another 15 minutes. After washing in 10 mM HEPES, pH 7.4, 140 mM NaCl and 2.5 mM CaCl₂, the retinas were labelled with M-Opsin antibody for 24 hours in 10 mM HEPES, pH 7.4, 140 mM NaCl, and 2.5 mM CaCl₂. The retinas were then washed and relabelled with the Alex-Fluor-594 (Molecular Probes, Eugene, OR, USA) secondary antibody. After labelling with the secondary antibody, the retinas were counter stained with DAPI, mounted on slides with the photoreceptor outer segments facing up, and photographed on a Zeiss LSM 800 confocal scanning microscope. For annexin V staining, Alex-Fluor-594-labelled annexin V (Molecular Probes, Eugene, OR, USA) was incubated with the retinas for 3 hours, and sections were counterstained with DAPI.

Cell culture

HEK-293T and COS7 cells (American Type Culture Collection (ATCC, Manassas, VA, USA) were seeded on coverslips and transiently cultured in DMEM medium with high glucose (HyClone) supplemented with 10% foetal bovine serum and 1% (vol/vol) penicillin/streptomycin at 37 °C in a 5% CO2 atmosphere. Cells were seeded in six-well plates (Corning, NY, USA) and transfected at 50% confluency with 1 µg of pCMV6-AN-Flag-Atp8a2, pCMV6-Tmem30a-HA or empty vectors using Lipofectamine 3000 (Invitrogen) according to the manufacturer’s instructions. Cells were harvested after 24–48 hours and fixed in 4% paraformaldehyde for 15 min at room temperature. After blocking with 1 × PBS containing 5% normal goat serum and 0.2% Triton X-100, cells were incubated with anti-Flag antibody (Sigma, St. Louis, MO, USA) and anti-HA antibody (Roche, Redwood city, CA, USA) at 4 °C overnight. Alexa-Fluor 594/488-conjugated secondary antibody (Invitrogen) was applied, and nuclei were counter stained with DAPI. Images were acquired with a confocal system (Leica) using a 63 × 1.4 NA oil immersion objective lens.

Mouse embryonic fibroblast (MEF) isolation

MEFs were isolated according to a previously reported protocol³⁹.

Lipid translocation assay

Lipid translocation assay was performed following previous published methods^{16, 22}.

The labeled phospholipid analog 16:0–06:0 NBD-PS [1-palmitoyl-2-[6-

[(7-nitro-2-1,3-benzoxadiazol-4-yl)amino] hexanoyl]-sn-glycero-3-

phospho-L-serine (ammonium salt)] were purchased from Avanti Polar Lipids (Alabaster, AL, USA). NBD-PS powder stocks were dissolved in 95% ethanol and diluted to 10 μM with Hank’s balanced salt solution with 15 mM MgCl₂ and without phenol red (HBSS-15 mM MgCl₂; Gibco). The isolated MEF cells were genotyped and cultured in DMEM high-glucose medium with 5 μg/ml tamoxifen for 48 hours. Cells with the genotypes of Tmem30a ^loxp/loxp were used as controls, and cells with the genotypes of Tmem30a ^loxp/loxp CAG-CreER were used as mutant cells. MEFs were seeded onto 60 mm-plates until they reached 80% confluency. Then, the cells were washed with PBS and treated with 0.25% trypsin. The cells were then suspended in PBS and centrifuged for 5 mins at 300 g followed by removal of the PBS buffer. The MEFs were then re-suspended with per-warmed 10 μM NBD-PS buffer in a 1.5-ml Eppendorf tube (Corning, NY, USA) and incubated for 15 minutes at 25 °C. Subsequently, the cells were centrifuged for 5 minutes at 300 g, and the supernatant was removed and immediately placed on ice. To quantify the NBD-lipids translocated into the inner leaflet of the plasma membrane, lipids from the outer leaflet were removed by back-extraction. This was done by adding ice-cold HBSS supplemented with 2% bovine serum albumin (Sigma, St Louis, MO, USA) to the cells for 10 minutes on ice, and then centrifuging the cells at 4 °C for 5 minutes at 300 g, and this process was repeated 3 times. Subsequently, the cells were suspended and subjected to FACS analysis.

Annexin V staining of MEFs

MEF cells were seeded onto 60 mm-plates with a polylysine-treated coverslip until they reached 60% confluency. The cells were washed with PBS and stained with annexin V in the staining buffer supplied with the testing kit. The cells were then washed with PBS three times and counterstained with DAPI.

Data Availability

All data generated or analysed during this study are included in this published article (and its supplemental information files).

References

Op den Kamp, J. A. Lipid asymmetry in membranes. Annual review of biochemistry 48, 47–71, doi:10.1146/annurev.bi.48.070179.000403 (1979).
Article CAS PubMed Google Scholar
Seigneuret, M. & Devaux, P. F. ATP-dependent asymmetric distribution of spin-labeled phospholipids in the erythrocyte membrane: relation to shape changes. Proceedings of the National Academy of Sciences of the United States of America 81, 3751–3755 (1984).
Article ADS CAS PubMed PubMed Central Google Scholar
Halleck, M. S. et al. Differential expression of putative transbilayer amphipath transporters. Physiological genomics 1, 139–150 (1999).
CAS PubMed Google Scholar
Holthuis, J. C. & Levine, T. P. Lipid traffic: floppy drives and a superhighway. Nature reviews. Molecular cell biology 6, 209–220, doi:10.1038/nrm1591 (2005).
Article CAS PubMed Google Scholar
Paulusma, C. C. & Oude Elferink, R. P. The type 4 subfamily of P-type ATPases, putative aminophospholipid translocases with a role in human disease. Biochimica et biophysica acta 1741, 11–24, doi:10.1016/j.bbadis.2005.04.006 (2005).
Article CAS PubMed Google Scholar
Tang, X., Halleck, M. S., Schlegel, R. A. & Williamson, P. A subfamily of P-type ATPases with aminophospholipid transporting activity. Science 272, 1495–1497 (1996).
Article ADS CAS PubMed Google Scholar
Leventis, P. A. & Grinstein, S. The distribution and function of phosphatidylserine in cellular membranes. Annual review of biophysics 39, 407–427, doi:10.1146/annurev.biophys.093008.131234 (2010).
Article CAS PubMed Google Scholar
Chen, C.-Y., Ingram, M. F., Rosal, P. H. & Graham, T. R. Role for Drs2p, a P-type ATPase and potential aminophospholipid translocase, in yeast late Golgi function. The Journal of cell biology 147, 1223–1236 (1999).
Article CAS PubMed PubMed Central Google Scholar
Darland-Ransom, M. et al. Role of C. elegans TAT-1 protein in maintaining plasma membrane phosphatidylserine asymmetry. Science 320, 528–531 (2008).
Article ADS CAS PubMed Google Scholar
Wang, L., Beserra, C. & Garbers, D. L. A novel aminophospholipid transporter exclusively expressed in spermatozoa is required for membrane lipid asymmetry and normal fertilization. Developmental biology 267, 203–215 (2004).
Article CAS PubMed Google Scholar
Bull, L. N. et al. A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Nature genetics 18, 219–224 (1998).
Article CAS PubMed Google Scholar
Cacciagli, P. et al. Disruption of the ATP8A2 gene in a patient with at (10; 13) de novo balanced translocation and a severe neurological phenotype. European Journal of Human Genetics 18, 1360–1363 (2010).
Article PubMed PubMed Central Google Scholar
Levano, K. et al. Atp8a1 deficiency is associated with phosphatidylserine externalization in hippocampus and delayed hippocampus‐dependent learning. Journal of neurochemistry 120, 302–313 (2012).
Article CAS PubMed Google Scholar
Martin-Hernandez, E. et al. New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy. Neurogenetics 17, 259–263, doi:10.1007/s10048-016-0496-y (2016).
Article CAS PubMed Google Scholar
Onat, O. E. et al. Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion. European journal of human genetics: EJHG 21, 281–285, doi:10.1038/ejhg.2012.170 (2013).
Article PubMed Google Scholar
Zhu, X. et al. Mutations in a P-type ATPase gene cause axonal degeneration. PLoS Genet 8, e1002853 (2012).
Article CAS PubMed PubMed Central Google Scholar
Meguro, M. et al. A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome. Nature genetics 28, 19–20 (2001).
CAS PubMed Google Scholar
Siggs, O. M. et al. The P4-type ATPase ATP11C is essential for B lymphopoiesis in adult bone marrow. Nature immunology 12, 434–440 (2011).
Article CAS PubMed PubMed Central Google Scholar
Yabas, M. et al. ATP11C is critical for the internalization of phosphatidylserine and differentiation of B lymphocytes. Nature immunology 12, 441–449, doi:10.1038/ni.2011 (2011).
Article CAS PubMed PubMed Central Google Scholar
Siggs, O. M., Schnabl, B., Webb, B. & Beutler, B. X-linked cholestasis in mouse due to mutations of the P4-ATPase ATP11C. Proceedings of the National Academy of Sciences of the United States of America 108, 7890–7895, doi:10.1073/pnas.1104631108 (2011).
Article ADS CAS PubMed PubMed Central Google Scholar
Yabas, M. et al. Mice deficient in the putative phospholipid flippase ATP11C exhibit altered erythrocyte shape, anemia, and reduced erythrocyte life span. The Journal of biological chemistry 289, 19531–19537, doi:10.1074/jbc.C114.570267 (2014).
Article CAS PubMed PubMed Central Google Scholar
Segawa, K. et al. Caspase-mediated cleavage of phospholipid flippase for apoptotic phosphatidylserine exposure. Science 344, 1164–1168, doi:10.1126/science.1252809 (2014).
Article ADS CAS PubMed Google Scholar
Bryde, S. et al. CDC50 proteins are critical components of the human class-1 P4-ATPase transport machinery. The Journal of biological chemistry 285, 40562–40572, doi:10.1074/jbc.M110.139543 (2010).
Article CAS PubMed PubMed Central Google Scholar
Paulusma, C. C. et al. ATP8B1 requires an accessory protein for endoplasmic reticulum exit and plasma membrane lipid flippase activity. Hepatology 47, 268–278, doi:10.1002/hep.21950 (2008).
Article CAS PubMed Google Scholar
Saito, K. et al. Cdc50p, a protein required for polarized growth, associates with the Drs2p P-type ATPase implicated in phospholipid translocation in Saccharomyces cerevisiae. Molecular biology of the cell 15, 3418–3432 (2004).
Article CAS PubMed PubMed Central Google Scholar
van der Velden, L. M. et al. Heteromeric interactions required for abundance and subcellular localization of human CDC50 proteins and class 1 P4-ATPases. The Journal of biological chemistry 285, 40088–40096, doi:10.1074/jbc.M110.139006 (2010).
Article PubMed PubMed Central Google Scholar
Folmer, D. et al. Cellular Localization and Biochemical Analysis of Mammalian CDC50A, a Glycosylated β-subunit for P4 ATPases. J Histochem Cytochem. 60(3), 205–218 (2012).
Article CAS PubMed PubMed Central Google Scholar
López-Marqués, R. L. et al. Intracellular targeting signals and lipid specificity determinants of the ALA/ALIS P4-ATPase complex reside in the catalytic ALA α-subunit. Molecular biology of the cell 21, 791–801 (2010).
Article PubMed PubMed Central Google Scholar
Coleman, J. A. & Molday, R. S. Critical role of the β-subunit CDC50A in the stable expression, assembly, subcellular localization, and lipid transport activity of the P4-ATPase ATP8A2. Journal of Biological Chemistry 286, 17205–17216 (2011).
Article CAS PubMed PubMed Central Google Scholar
Lenoir, G., Williamson, P., Puts, C. F. & Holthuis, J. C. Cdc50p plays a vital role in the ATPase reaction cycle of the putative aminophospholipid transporter Drs2p. Journal of biological chemistry 284, 17956–17967 (2009).
Article CAS PubMed PubMed Central Google Scholar
Coleman, J. A. et al. Phospholipid flippase ATP8A2 is required for normal visual and auditory function and photoreceptor and spiral ganglion cell survival. Journal of cell science 127, 1138–1149, doi:10.1242/jcs.145052 (2014).
Article CAS PubMed PubMed Central Google Scholar
Coleman, J. A., Kwok, M. C. & Molday, R. S. Localization, purification, and functional reconstitution of the P4-ATPase Atp8a2, a phosphatidylserine flippase in photoreceptor disc membranes. The Journal of biological chemistry 284, 32670–32679, doi:10.1074/jbc.M109.047415 (2009).
Article CAS PubMed PubMed Central Google Scholar
Farley, F. W., Soriano, P., Steffen, L. S. & Dymecki, S. M. Widespread recombinase expression using FLPeR (flipper) mice. Genesis (New York, N.Y.: 2000) 28, 106–110 (2000).
Tronche, F. et al. Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety. Nat Genet 23, 99–103, doi:10.1038/12703 (1999).
Article CAS PubMed Google Scholar
Furuta, Y., Lagutin, O., Hogan, B. L. & Oliver, G. C. Retina- and ventral forebrain-specific Cre recombinase activity in transgenic mice. Genesis (New York, N.Y.: 2000) 26, 130–132 (2000).
Article CAS Google Scholar
Le, Y.-Z. et al. Targeted expression of Cre recombinase to cone photoreceptors in transgenic mice. Mol Vis 10, 1011–1018 (2004).
CAS PubMed Google Scholar
Hayashi, S. & McMahon, A. P. Efficient recombination in diverse tissues by a tamoxifen-inducible form of Cre: a tool for temporally regulated gene activation/inactivation in the mouse. Dev Biol 244, 305–318, doi:10.1006/dbio.2002.0597 (2002).
Article CAS PubMed Google Scholar
Madisen, L. et al. A robust and high-throughput Cre reporting and characterization system for the whole mouse brain. Nat Neurosci 13(1), 133–40 (2010).
Article CAS PubMed Google Scholar
Dong, S., Maziveyi, M. & Alahari, S. K. Primary Tumor and MEF Cell Isolation to Study Lung Metastasis. JoVE (Journal of Visualized Experiments), e52609–e52609 (2015).

Download references

Acknowledgements

The authors want to thank the patients for their participation. The authors also want to thank Dr. Robert Molday for generously providing TMEM30A, ATP8A2, and 1D1, 1D4 antibodies, Dr. Simon SW John for providing the vmd mouse line and Dr. Y.Z. Le for providing the HRGP-Cre (cone-Cre) mouse line. This study was supported by grants from the Natural Science Foundation of China (81470668, 81271007, [XJ.Zhu.], 81670877 [F.Lu]), the Department of Science and Technology of Sichuan Province (2016TD0009, 2017TJPT0010, 2015SC0060, 2014FZ0122 [XJ.Zhu]), and the Sichuan Provincial Outstanding Youth Research Grant (2014JQ0023 [XJ.Zhu]), grant from China Postdoctoral Science Foundation (2016M600734) to Lin Zhang. The authors alone are responsible for the content and the writing of the paper.

Author information

Lin Zhang and Yeming Yang contributed equally to this work.

Authors and Affiliations

Sichuan Provincial Key Laboratory for Human Disease Gene Study and School of Medicine, Hospital of the University of Electronic Science and Technology of China and Sichuan Provincial People’s Hospital, Chengdu, Sichuan, 610072, China
Lin Zhang, Yeming Yang, Shujin Li, Shanshan Zhang, Xiong Zhu, Zhengfu Tai, Mu Yang, Yuqing Liu, Zhilin Jiang, Fang Lu & Xianjun Zhu
Department of Laboratory Medicine, Sichuan Academy of Medical Sciences and Sichuan Provincial People’s Hospital, Chengdu, Sichuan, 610072, China
Lin Zhang, Yeming Yang, Yuqing Liu, Fang Lu & Xianjun Zhu
Institute of Laboratory Animal Sciences, Sichuan Academy of Medical Sciences and Sichuan Provincial People’s Hospital, Chengdu, Sichuan, China
Xianjun Zhu
Chengdu Institute of Biology, Chinese Academy of Sciences Sichuan Translational Medicine Research Hospital, Chengdu, Sichuan, China
Shujin Li, Zhengfu Tai, Mu Yang & Xianjun Zhu
Department of Ophthalmology, Yale University School of Medicine, New Haven, CT, USA
Xinzheng Guo & Bo Chen

Authors

Lin Zhang
View author publications
You can also search for this author in PubMed Google Scholar
Yeming Yang
View author publications
You can also search for this author in PubMed Google Scholar
Shujin Li
View author publications
You can also search for this author in PubMed Google Scholar
Shanshan Zhang
View author publications
You can also search for this author in PubMed Google Scholar
Xiong Zhu
View author publications
You can also search for this author in PubMed Google Scholar
Zhengfu Tai
View author publications
You can also search for this author in PubMed Google Scholar
Mu Yang
View author publications
You can also search for this author in PubMed Google Scholar
Yuqing Liu
View author publications
You can also search for this author in PubMed Google Scholar
Xinzheng Guo
View author publications
You can also search for this author in PubMed Google Scholar
Bo Chen
View author publications
You can also search for this author in PubMed Google Scholar
Zhilin Jiang
View author publications
You can also search for this author in PubMed Google Scholar
Fang Lu
View author publications
You can also search for this author in PubMed Google Scholar
Xianjun Zhu
View author publications
You can also search for this author in PubMed Google Scholar

Contributions

X.J. Zhu conceived and designed the experiments; L. Zhang, Y. Yang, S. Li, S. Zhang, M. Yang, X. Zhu, Z. Tai, Y. Liu, X. Guo, B. Chen and Z. Jiang conducted the experiments and analysed the data; X.J. Zhu and F. Lu supervised the experiment and wrote the paper with input from L. Zhang and Y. Yang.

Corresponding authors

Correspondence to Fang Lu or Xianjun Zhu.

Ethics declarations

Competing Interests

The authors declare that they have no competing interests.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Supplementary data

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Cite this article

Zhang, L., Yang, Y., Li, S. et al. Loss of Tmem30a leads to photoreceptor degeneration. Sci Rep 7, 9296 (2017). https://doi.org/10.1038/s41598-017-09506-5

Download citation

Received: 21 April 2017
Accepted: 26 July 2017
Published: 24 August 2017
DOI: https://doi.org/10.1038/s41598-017-09506-5

This article is cited by

Knockdown of TMEM30A in renal tubular epithelial cells leads to reduced glucose absorption
- Sipei Chen
- Xinrou Song
- Guisen Li
BMC Nephrology (2023)
TMEM30A is essential for hair cell polarity maintenance in postnatal mouse cochlea
- Yazhi Xing
- Kun Peng
- Shankai Yin
Cellular & Molecular Biology Letters (2023)
Disruption of Tmem30a results in cerebellar ataxia and degeneration of Purkinje cells
- Yeming Yang
- Kuanxiang Sun
- Xianjun Zhu
Cell Death & Disease (2018)

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.