- Article
- Published:
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome
- Carolyn J. Brown1,
- Andrea Ballabio1 na1,
- James L. Rupert1,
- Ronald G. Lafreniere1,
- Markus Grompe1 na1,
- Rossana Tonlorenzi1 na1 &
- …
- Huntington F. Willard1 na2
Naturevolume 349, pages38–44 (1991)Cite this article
6413Accesses
32Altmetric
Abstract
X-chromosome inactivation results in thecis-limited dosage compensation of genes on one of the pair of X chromosomes in mammalian females. Although most X-linked genes are believed to be subject to inactivation, several are known to be expressed from both active and inactive X chromosomes. Here we describe an X-linked gene with a novel expression pattern—transcripts are detected only from the inactive X chromosome (Xi) and not from the active X chromosome (Xa). This gene, calledXIST (for Xi-specific transcripts), is a candidate for a gene either involved in or uniquely influenced by the process of X inactivation.
This is a preview of subscription content,access via your institution
Access options
Subscription info for Japanese customers
We have a dedicated website for our Japanese customers. Please go tonatureasia.com to subscribe to this journal.
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Lyon, M. F.Biol. Rev.47, 1–35 (1972).
Gartler, S. M. & Riggs, A. D.A. Rev. Genet.17, 155–190 (1983).
Lyon, M. F.Nature190, 372–373 (1961).
Russell, L. B.Science140, 976–978 (1963).
Cattanach, B. M.A. Rev. Genet.9, 1–18 (1975).
Migeon, B. R., der Kaloustian, V. M., Nyhan, W. L., Young, W. J. & Childs, B.Science160, 425–427 (1968).
Meyer, W. J., Migeon, B. R. & Migeon, C. J.Proc. natn. Acad. Sci. U.S.A.72, 1469–1472 (1975).
Davidson, R. G., Nitowsky, H. M. & Childs, B.Proc. natn. Acad. Sci. U.S.A.50, 481–484 (1963).
Schneider-Gadicke, A., Beer-Romero, P., Brown, L. G., Nussbaum, R. & Page, D. C.Cell57, 1247–1258 (1989).
Fisher, E.et al.Cell63, 1205–1218 (1990).
Nadon, N., Dorn, N. & DeMars, R.Somat. Cell molec. Genet.14, 541–552 (1988).
Graves, J. A. M. & Gartler, S. M.Somat. Cell. molec. Genet.12, 275–280 (1986).
Brown, C. J., Flenniken, A., Williams, B. & Willard, H. F.Nucleic Acids Res.18, 4191–4195 (1990).
Shapiro, L. J., Mohandas, T., Weiss, R. & Romeo, G.Science204, 1224–1226 (1979).
Goodfellow, P., Pym, B., Mohandas, T. & Shapiro, L. J.Am. J. hum. Genet.36, 777–782 (1984).
Brown, C. J. & Willard, H. F.Am. J. hum. Genet.46, 273–279 (1990).
Brown, C. J., Barker, D. & Willard, H. F.Am. J. hum. Genet.45, A178 (1989).
Ballabio, A.et al.Proc. natn. Acad Sci. U.S.A.84, 4519–4523 (1987).
Brown, C. J.et al.Nature349, 82–84 (1991).
Migeon, B. R., Sprenkle, J. A. & Do, T. T.Cell18, 637–641 (1979).
Willard, H. F. & Breg, W. R.Somat. Cell Genet.6, 187–188 (1980).
Shapiro, M. B. & Senapathy, P.Nucleic Acids Res.15, 7155–7175 (1987).
Frohman, M. A., Dush, M. K. & Martin, G. R.Proc. natn. Acad. Sci. U.S.A.85, 8998–9002 (1988).
Fickett, J. W.Nucleic Acids Res.10, 5303–531 (1982).
Mattel, M. G., Mattel, J. F., Vidal, I. & Giraud, F.Hum. Genet.56, 401–408 (1981).
Summitt, R. L., Tipton, R. E., Wilroy, R. S. Jr., Martens, P. & Phelan, J. P.Birth Defects: Orig. Art. Ser.14, 219–247 (1978).
Therman, E., Sarto, G. E. & Patau, K.Chromosoma44, 361–366 (1974).
Fiejter, W. L., Van Dyke, D. L. & Weiss, L.Am. J. hum. Genet.36, 218–226 (1984).
Rastan, S.J. Embryol. exp. Morph.78, 1–22 (1983).
Rastan, S. & Robertson, E. J.J. Embryol. exp. Morph.90, 379–388 (1985).
Johnston, P. G. & Cattanach, B. M.Genet. Res.37, 151–160 (1981).
Rastan, S.Genet Res.40, 139–147 (1982).
Brown, S. W. & Chandra, H. S.Proc. natn. Acad. Sci. U.S.A.70, 195–199 (1973).
Riggs, A. D.Aust. J. Zool.37, 419–441 (1990).
Lyon, M. F.et al.J. Embryol. exp. Morph.97, 75–85 (1986).
Keer, J. T.et al.Genomics7, 566–572 (1990).
Chirgwin, J. M.et al.Biochemistry18, 5294–5299 (1979).
Brown, C. J. & Willard, H. F.Am. J. hum. Genet.45, 592–598 (1989).
Grompe, M., Muzny, D. M. & Caskey, C. T.Proc. natn. Acad. Sci. U.S.A.86, 5888–5892 (1989).
Korneluk, R. G., Quan, F. & Gravel, R. A.Gene40, 317–323 (1985).
Gibbs, R. A., Nguyen, P.-N., McBride, L. J., Koepf, S. M. & Caskey, C. T.Proc. natn. Acad. Sci. U.S.A.86, 1919–1923 (1989).
Author information
Andrea Ballabio, Markus Grompe and Rossana Tonlorenzi: Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030, USA
Huntington F. Willard: To whom correspondence should be addressed.
Authors and Affiliations
Department of Genetics, Stanford University School of Medicine, Stanford, California, 94305, USA
Carolyn J. Brown, Andrea Ballabio, James L. Rupert, Ronald G. Lafreniere, Markus Grompe, Rossana Tonlorenzi & Huntington F. Willard
- Carolyn J. Brown
You can also search for this author inPubMed Google Scholar
- Andrea Ballabio
You can also search for this author inPubMed Google Scholar
- James L. Rupert
You can also search for this author inPubMed Google Scholar
- Ronald G. Lafreniere
You can also search for this author inPubMed Google Scholar
- Markus Grompe
You can also search for this author inPubMed Google Scholar
- Rossana Tonlorenzi
You can also search for this author inPubMed Google Scholar
- Huntington F. Willard
You can also search for this author inPubMed Google Scholar
Rights and permissions
About this article
Cite this article
Brown, C., Ballabio, A., Rupert, J.et al. A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome.Nature349, 38–44 (1991). https://doi.org/10.1038/349038a0
Received:
Accepted:
Issue Date:
Share this article
Anyone you share the following link with will be able to read this content:
Sorry, a shareable link is not currently available for this article.
Provided by the Springer Nature SharedIt content-sharing initiative
This article is cited by
X chromosome inactivation skewing is common in advanced carotid atherosclerotic lesions in females and predicts secondary peripheral artery events
- Michele F. Buono
- Ernest Diez Benavente
- Hester M. den Ruijter
Biology of Sex Differences (2023)
LncRNA XIST regulates breast cancer stem cells by activating proinflammatory IL-6/STAT3 signaling
- Yuxi Ma
- Yongyou Zhu
- Ming Luo
Oncogene (2023)
GATA transcription factors drive initial Xist upregulation after fertilization through direct activation of long-range enhancers
- Liat Ravid Lustig
- Abhishek Sampath Kumar
- Edda G. Schulz
Nature Cell Biology (2023)
Multiple distinct domains of human XIST are required to coordinate gene silencing and subsequent heterochromatin formation
- Thomas Dixon-McDougall
- Carolyn J. Brown
Epigenetics & Chromatin (2022)
In vitro production of desired sex ovine embryos modulating polarity of oocytes for sex-specific sperm binding during fertilization
- Ramesh Kumar G.
- Ashish Mishra
- Raghavendra Bhatta
Scientific Reports (2022)