Abstract
The human genome is rich in sequences which are structurally related to the 7SL RNA component of the signal recognition particle1. The 7SL DNA sequence family consists of four 7SL genes2, 500 7SL pseudogenes2 (which are truncated at one or both ends of the 7SL sequence) and 500,000 Alu sequences3–5. Both 7SL genes2 and Alu elements6–8 are transcribed by RNA polymerase III, and we show here that the internal 7SL promoter lies within the Alu-like part of the 7SL gene. Why then does RNA polymerase III transcribe the few 7SL genes so efficiently, while transcripts from the far more abundant Alu elements are not readily detectable9–11? We find that a human 7SL gene and a synthetic Alu sequence derived from it are expressed 50–100-fold more efficiently in vitro than either a representative Alu element or two 7SL pseudogenes. 5′ Deletion and insertion mutants of the 7SL gene demonstrate that, in conjunction with the internal promoter, the first 37 nucleotides upstream from the transcription start site are essential for efficient and accurate initiation in vitro. We suggest that the genomic sequences upstream from most Alu elements and 7SL pseudogenes do not contain this element, and consequently that only a small subset of such sequences can be transcribed in vivo. This may help to explain the homogeneity of the Alu family within each mammalian genome, as well as the species-specific differences between mammalian Alu families.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Walter, P. & Bobel, G. Nature 299, 691–698 (1982).
Ullu, E. & Weiner, A. M. EMBO J. 3, 3303–3310 (1984).
Houck, C. M., Rinehart, F. P. & Schmid, C. W. J. molec. Biol. 132, 289–306 (1979).
Ullu, E. & Tschudi, C. Nature 312, 171–172 (1984).
Gundelfinger, E. D., Di Carlo, M., Zopf, D. & Melli, M. L. EMBO J. 3, 2325–2332 (1984).
Duncan, C. H., Jagadeeswaran, P., Wang, R. R. C. & Weissman, S. H. Gene 13, 185–196 (1981).
Paolella, G., Lucero, M. A., Murphy, M. H. & Baralle, F. EMBO J. 2, 691–696 (1983).
Perez-Stable, C., Ayres, T. M. & Shen, C. J. Proc. natn. Acad. Sci. U.S.A. 81, 5291–5295 (1984).
Haynes, S. R. & Jelinek, W. R. Proc. natn. Acad. Sci U.S.A. 78, 6130–6134 (1981).
Young, P. R., Scott, R. W., Homer, D. H. & Tilghman, S. M. Nucleic Acids Res. 10, 3099–3116 (1982).
Allan, M. & Paul, J. Nucleic Acids Res. 12, 1193–1200 (1984).
Ullu, E., Murphy, S. & Melli, M. Cell 29, 195–202 (1982).
Van Arsdell, S. W. et al. Cell 26, 11–17 (1981).
Jagadeeswaran, P., Forget, B. G. & Weissman, S. M. Cell 26, 141–142 (1981).
Sakonju, S., Bogenhagen, D. F. & Brown, D. D. Cell 19, 13–25 (1980).
Hofstetter, H., Kressmann, A. & Birnstiel, M. L. Cell 24, 573–585 (1981).
Fowlkes, D. M. & Shenk, T. Cell 22, 405–413 (1980).
Larson, D., Bradford-Wilcox, J., Young, L. S. & Sprague, K. U. Proc. natn. Acad. Sci. U.S.A. 80, 3416–3420 (1983).
Raymond, G. J. & Johnson, J. D. Nucleic Acids Res. 11, 5969–5988 (1983).
Morton, D. G. & Sprague, K. U. Proc. natn. Acad. Sci. U.S.A. 81, 5519–5522 (1984).
Shaw, K. J. & Olson, M. V. Molec. cell. Biol. 4, 657–665 (1984).
Schaack, J. et al. J. biol. Chem. 259, 1461–1467 (1984).
De Franco, D., Schmidt, O. & Söll, D. Proc. natn. Acad. Sci. U.S.A. 77, 3365–3368 (1980).
Dingermann, T., Burke, D. J., Sharp, S., Shaack, J. & Söll, D. J. biol. Chem. 257, 14738–14744 (1982).
Hipskind, R. A. & Clarkson, S. G. Cell 34, 881–890 (1983).
Krayev, A. S. et al. Nucleic Acids Res. 8, 1201–1215 (1980).
Haynes, S. R., Toomey, T. P., Leinwand, L. & Jelinek, W. R. Molec. cell. Biol. 1, 573–583 (1981).
Deininger, P. L., Jolly, D. J., Rubin, C. M., Friedmann, T. & Schmid, C. W. J. molec. Biol. 151, 17–33 (1981).
Daniels, G. R., Fox, G. M., Loewensteiner, D., Schmid, C. W. & Deininger, P. L. Nucleic Acids Res. 11, 7569–7593 (1983).
Weiner, A. M., Deininger, P. L. & Efstradiatis, A. A. Rev. Biochem. 55 (in the press).
Dignam, J. D., Lebovitz, R. M. & Roeder, R. G. Nucleic Acids Res. 11, 1475–1489 (1983).
Bogenhagen, D. F. & Brown, D. D. Cell 24, 261–270 (1981).
Ullu, E. & Melli, M. L. Nucleic Acids Res. 10, 2209–2223 (1982).
Grimaldi, G., Queen, C. & Singer, M. Nucleic Acids Res. 21, 5553–5567 (1981).
Maxam, A. M. & Gilbert, W. Meth. Enzym. 65, 499–560 (1980).
Ciliberto, G., Raugei, G., Costanzo, F., Dente, L. & Cortese, R. Cell 32, 725–733 (1983).
Heffron, F., So, M. & McCarthy, B. J. Proc. natn. Acad. Sci. U.S.A. 75, 6012–6016 (1978).
Hernandez, N. & Keller, W. Cell 35, 89–99 (1983).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Ullu, E., Weiner, A. Upstream sequences modulate the internal promoter of the human 7SL RNA gene. Nature 318, 371–374 (1985). https://doi.org/10.1038/318371a0
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1038/318371a0
This article is cited by
-
Orangutan Alu quiescence reveals possible source element: support for ancient backseat drivers
Mobile DNA (2012)
-
Novel TRF1/BRF target genes revealed by genome-wide analysis of Drosophila Pol III transcription
The EMBO Journal (2007)
-
On the Possibility of Origin of a Short Element of Drosophila (Suffix) from a Related Long Retroelement (F Element)
Doklady Biochemistry and Biophysics (2005)
-
LINE-mediated retrotransposition of marked Alu sequences
Nature Genetics (2003)
-
Molecular analysis of the gene family of the signal recognition particle (SRP) RNA of tomato
Plant Molecular Biology (1996)
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.