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Low-copy-number human transgene is recognized as an X inactivation center in mouse ES cells, but fails to induce cis-inactivation in chimeric mice.
- Source :
-
Genomics [Genomics] 2001 Jan 15; Vol. 71 (2), pp. 156-62. - Publication Year :
- 2001
-
Abstract
- X chromosome inactivation is initiated from a segment of the mammalian X chromosome called the X inactivation center. Transgenes from this region of the murine X chromosome are providing the means to identify the DNA needed for cis inactivation in mice. We recently showed that chimeric mice carrying transgenes from the human X inactivation center (XIC) region also provide a functional assay for human XIC activity; approximately 6 copies of a 480-kb human transgene (ES-10) were sufficient to initiate random X inactivation in cells of male chimeric mice (Migeon et al., 1999, Genomics, 59, 113-121). Now, we report studies of another human transgene (ES-5), which contains less than 300 kb of the human XIC region on Xq13.2 including an intact XIST locus and which has inserted in one or two copies into mouse chromosome 6. The ES-5 transgene is recognized as an X inactivation center in mouse embryonic stem cells, but is not sufficient to induce random X inactivation in somatic cells of highly chimeric mice. Human transgenes in chimeric mice provide a means to uncouple the key steps in this complex pathway and facilitate the search for essential components of the human XIC region.<br /> (Copyright 2001 Academic Press.)
- Subjects :
- Animals
Cells, Cultured
Chimera genetics
Clone Cells
Embryo, Mammalian cytology
Female
Fetal Death genetics
Humans
Male
Mice
Mice, Transgenic
RNA metabolism
RNA, Long Noncoding
RNA, Untranslated genetics
Stem Cells metabolism
Transcription Factors genetics
Transfection
Dosage Compensation, Genetic
Gene Dosage
Transgenes genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0888-7543
- Volume :
- 71
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Genomics
- Publication Type :
- Academic Journal
- Accession number :
- 11161809
- Full Text :
- https://doi.org/10.1006/geno.2000.6421