Chromosomal basis of X chromosome inactivation: Identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation

  1. Andrew P. Miller* and
  2. Huntington F. Willard
  1. Department of Genetics and Center for Human Genetics, Case Western Reserve University School of Medicine and University Hospitals of Cleveland, Cleveland, OH 44106
  1. 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. AF069134AF069138).

  • ABBREVIATIONS:
    Mb,
    megabase;
    YAC,
    yeast artificial chromosome;
    EST,
    expressed sequence tag;
    STS,
    sequence-tagged site;
    RT-PCR,
    reverse transcription–PCR
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