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Endosperm-specific demethylation and activation of specific alleles of α-tubulin genes of Zea mays L.

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Abstract

We have investigated the methylation status of the α-tubulin genes, and the degree of accumulation of their mRNAs in endosperm, embryo and seedling tissues of Zea mays L. We have found that many of the α-tubulin genes are differentially demethylated in the endosperm relative to the embryo and seedling. However, only for tubα2 and tubα4 could a correlation between DNA demethylation and increased RNA accumulation be detected. By analyzing the inbred lines W64A and A69Y and their reciprocal crosses, we have also identified in the endosperm two α-tubulin genes, tubα3 and tubα4, that are differentially demethylated if transmitted by the maternal germline, but that remain hypermethylated when transmitted by the paternal germline.

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References

  • Amos LA (1979) Structure of microtubules. In: Roberts K, Hyans IS (eds) Microtubules. Academic Press, London, pp 1–64

    Google Scholar 

  • Bartolomei MS, Webber AL, Brunkow ME, Tilghman SM (1993) Epigenetic mechanisms underlying the imprinting of the mouse H19 gene. Genes Dev 7:1663–1673

    Google Scholar 

  • Bianchi MW, Viotti A (1988) DNA methylation and tissuespecific transcription of storage protein genes of maize. Plant Mol Biol 11: 203–214

    Google Scholar 

  • Brandeis M, Kafri T, Ariel M, Chaillet JR, McCarrey J, Razin A, Cedar H (1993) The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. EMBO J 12:3669–3677

    Google Scholar 

  • Brink RA, Cooper DC (1947) The endosperm in seed development. Bot Rev 13:423–541

    Google Scholar 

  • Brink RA, Kermicle JL, Ziebur NK (1970) Derepression in the female gametophyte in relation to paramutant R expression in maize endosperms, embryos and seedlings. Genetics 66: 87–96

    Google Scholar 

  • Chaudhuri S, Messing J (1994) Allele-specific parental imprinting of dzrl, a posttranscriptional regulator of zein accumulation. Proc Natl Acad Sci USA 91:4867–4871

    Google Scholar 

  • Das OP, Messing J (1994) Variegated phenotype and developmental methylation changes of a maize allele originating from epimutation. Genetics 136:1121–1141

    Google Scholar 

  • Ferguson-Smith AC, Sasaki H, Cattanach BM, Surani MA (1993) Parental-origin-specific epigenetic modification of the mouse H19 gene. Nature 362: 751–755

    Google Scholar 

  • Flavell RB, O'Dell M (1990) Variation and inheritance of cytosine methylation in ribosomal DNA and nucleolus organizer expression in wheat. Plant Mol Biol 11:203–214

    Google Scholar 

  • Fosket OE, Morejohn LC (1992) Structural and functional organization of tubulin. Annu Rev Plant Physiol 43:201–240

    Google Scholar 

  • Goddard RH, Wick SM, Silflow CD, Snustad DP (1994) Microtubule components of the plant cell cytoskeleton. Plant Physiol 104:1–6

    Google Scholar 

  • Gunning BES, Hardham AR (1982) Microtubules. Annu Rev Plant Physiol 33:651–698

    Google Scholar 

  • Haig D, Westoby M (1991) Genomic imprinting in endosperm: effects on seed development in crosses between species, and between different ploidies of the same species and its implications for the evolution of apomixis. Philos Trans R Soc Lond [Biol] 333: 1–13

    Google Scholar 

  • Joyce CM, Villemur R, Snustad DP, Silflow CD (1992) Tubulin gene expression in maize (Zea mays) Change in isotype expression along the developmental axis of seedling root. J Mol Biol 227:97–107

    Google Scholar 

  • Kaufmann LS, Watson JC, Thompson WF (1987) Light regulated changes in DNase I hypersensitive sites in the rRNA genes of Pisum sativum. Proc Natl Acad Sci USA 84:1550–1554

    Google Scholar 

  • Kermicle JL (1970) Dependence of the R-mottled aleurone phenotype in maize on mode of sexual transmission. Genetics 66: 69–85

    Google Scholar 

  • Kopczak SD, Haas NA, Hussey PJ, Silflow CD, Snustad DP (1992) The small genome of Arabidopsis thaliana contains at least six expressed α-tubulin genes. Plant Cell 4:539–547

    Google Scholar 

  • Kowles RV, Phillips RL (1985) DNA amplification patterns in maize endosperm nuclei during kernel development. Proc Natl Acad Sci USA 82:7010–7014

    Google Scholar 

  • Langdale JA, Taylor WC, Nelson T (1991) Cell-specific accumulation of maize phosphoenol-pyruvate carboxylase is correlated with demethylation at a specific site >3 kb upstream of the gene. Mol Gen Genet 225:49–55

    Google Scholar 

  • Matzke MA, Matzke AIM (1991) Differential inactivation and methylation of a transgene in plants by two suppressor loci containing homologous sequences. Plant Mol Biol 16: 821–830

    Google Scholar 

  • Mereghetti M, Consonni G, Tonelli C (1990) A cDNA clone of the maize α-tubulin. Maize Genet Coop Newslett 64:87–88

    Google Scholar 

  • Meyer P, Heidmann I, Niedenhoff I (1993) Differences in DNA methylation are associated with a paramutation phenomenon in transgenic petunia. Plant J 4: 89–100

    Google Scholar 

  • Mitchinson T, Kirschner M (1984) Microtubule assembly nucleated by isolated centrosomes. Nature 312: 232–237

    Google Scholar 

  • Montoliu L, Rigau J, Puigdomenech P (1989) A tandem of α-tubulin genes preferentially expressed in radicular tissues from Zea mays. Plant Mol Biol 14:1–15

    Google Scholar 

  • Montoliu L, Puigdomenech P, Rigau J (1990) The tubα3 gene from Zea mays: structure and expression in dividing plant tissues. Gene 94: 201–207

    Google Scholar 

  • Morejohn LC (1991) The molecular pharmacology of plant tubulin and microtubules. In: Lloyd CW (ed) The cytoskeletal basis of plant growth and form. Academic Press, London pp 29–43

    Google Scholar 

  • Riggs CD, Chrispeels MJ (1990) The expression of phytohemagglutinin genes in Phaesolus vulgaris is associated with organspecific DNA methylation patterns. Plant Mol Biol 14:629–632

    Google Scholar 

  • Sasaki H, Jones PA, Chaillet JR, Ferguson-Smith AC, Barton SC, Reik W, Surani MA (1992) Parental imprinting: potentially active chomatin of the repressed maternal allele of the mouse insulin-like growth factor H (Igf-2) gene. Genes Dev 6: 1843–1856

    Google Scholar 

  • Schläppi M, Raina R, Fedoroff N (1994) Epigenetic regulation of the maize Spm transposable element: novel activation of a methylated promoter by TnpA. Cell 77:427–437

    Google Scholar 

  • Silflow CD, Oppenheimer DG, Kopczak SD, Ploense SE, Ludwig SR, Haas N, Snustad DP (1987) Plant tubulin genes: structure and differential expression during development. Dev Genet 8:435–460

    Google Scholar 

  • Sørensen MB (1992) Methylation of B-hordein genes in barley endosperm is inversely correlated with gene activity and affected by the regulatory gene Lys3. Proc Natl Acad Sci USA 89:4119–4123

    Google Scholar 

  • Snustad DD, Haas NA, Kopczak SD, Silflow CD (1992) The small genome of Arabidopsis thaliana contains at least six expressed β-tubulin genes. Plant Cell 4: 549–556

    Google Scholar 

  • Stöger R, Kubicka P, Liu C-G, Kafri T, Razin A, Cedar H, Barlow DP (1993) Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. Cell 73: 61–71

    Google Scholar 

  • Villemur R, Joyce CM, Haas NA, Goddard RH, Kopczak SD, Hussey PJ, Snustad DP, Silflow CD (1992) α-tubulin gene amily of maize (Zea mays L.) Evidence for two ancient α-tubulin genes in plants. J Mol Biol 227: 81–96

    Google Scholar 

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Communicated by H. Saedler

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Lund, G., Messing, J. & Viotti, A. Endosperm-specific demethylation and activation of specific alleles of α-tubulin genes of Zea mays L.. Molec. Gen. Genet. 246, 716–722 (1995). https://doi.org/10.1007/BF00290717

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  • DOI: https://doi.org/10.1007/BF00290717

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