Chromosomal basis of X chromosome inactivation: Identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation
- Department of Genetics and Center for Human Genetics, Case Western Reserve University School of Medicine and University Hospitals of Cleveland, Cleveland, OH 44106
-
Communicated by Shirley M. Tilghman, Princeton University, Princeton, NJ (received for review January 30, 1998)
Abstract
A number of genes have been identified that escape mammalian X chromosome inactivation and are expressed from both active and inactive X chromosomes. The basis for escape from inactivation is unknown and, a priori, could be a result of local factors that act in a gene-specific manner or of chromosomal control elements that act regionally. Models invoking the latter predict that such genes should be clustered in specific domains on the X chromosome, rather than distributed at random along the length of the X. To distinguish between these possibilities, we have constructed a transcription map composed of at least 23 distinct expressed sequences in an ≈5.5-megabase region on the human X chromosome spanning Xp11.21-p11.22. The inactivation status of these transcribed sequences has been determined in a somatic cell hybrid system and correlated with the position of the genes on the physical map. Although the majority of transcribed sequences in this region are subject to X inactivation, eight expressed sequences (representing at least six different genes) escape inactivation, and all are localized to within a region of less than 370 kb. Genes located both distal and proximal to this cluster are subject to inactivation, thereby defining a unique multigene domain on the proximal short arm that is transcriptionally active on the inactive X chromosome.
Footnotes
-
↵ * Present address: Sequana Therapeutics, 11099 North Torrey Pines Road, Suite 160, La Jolla, CA 92037. e-mail: andrew_miller{at}sequana.com.
-
↵ † To whom reprint requests should be addressed at: Department of Genetics, Case Western Reserve University School of Medicine, 2109 Adelbert Road, Cleveland, OH 44106-4955. e-mail: hfw{at}po.cwru.edu.
-
Data deposition: The sequences reported in this paper have been deposited in the GenBank database (accession nos. AF069134–AF069138).
- ABBREVIATIONS:
- Mb,
- megabase;
- YAC,
- yeast artificial chromosome;
- EST,
- expressed sequence tag;
- STS,
- sequence-tagged site;
- RT-PCR,
- reverse transcription–PCR
- Copyright © 1998, The National Academy of Sciences





