doi: 10.1016/0888-7543(90)90200-e.
Genetic mapping in the region of the mouse X-inactivation center
Affiliations
- PMID: 1974879
- DOI: 10.1016/0888-7543(90)90200-e
Item in Clipboard
Genetic mapping in the region of the mouse X-inactivation center
Genomics.
1990 Aug.
Abstract
The mouse X-inactivation center lies just distal to the T16H breakpoint. Utilizing pedigree analysis of backcross progeny from a Mus domesticus/Mus spretus interspecific cross, we have mapped a number of genetic loci, gene probes, microclones, and EagI linking clones distal to the T16H breakpoint. The genetic analysis provides a detailed genetic map in the vicinity of the mouse X-inactivation center. Comparative mapping data from the human X chromosome indicate that the most probable location of the mouse X-inactivation center is distal to Ccg-1 and in the region of the Pgk-1 locus. We report the assignment of two new loci, EM13 and DXSmh44, to the Ccg-1/Pgk-1 interval.
Similar articles
-
High-density molecular map of the central span of the mouse X chromosome.Genomics. 1991 May;10(1):17-22. doi: 10.1016/0888-7543(91)90478-w. Genomics. 1991. PMID: 1675191
-
Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crosses.EMBO J. 1987 Nov;6(11):3291-7. doi: 10.1002/j.1460-2075.1987.tb02648.x. EMBO J. 1987. PMID: 2448136 Free PMC article.
-
Determination of a molecular map position for Hyp using a new interspecific backcross produced by in vitro fertilization.Genomics. 1991 Nov;11(3):651-7. doi: 10.1016/0888-7543(91)90072-m. Genomics. 1991. PMID: 1685478
-
Development and applications of a molecular genetic linkage map of the mouse genome.Trends Genet. 1991 Apr;7(4):113-8. doi: 10.1016/0168-9525(91)90455-y. Trends Genet. 1991. PMID: 2068781 Review.
-
Genetic analysis of the mouse using interspecific crosses.Trends Genet. 1988 Jan;4(1):18-23. doi: 10.1016/0168-9525(88)90123-0. Trends Genet. 1988. PMID: 3070850 Review. No abstract available.
Cited by
-
Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1.Am J Hum Genet. 1991 Jun;48(6):1133-8. Am J Hum Genet. 1991. PMID: 2035533 Free PMC article.
-
Mapping of a mouse homolog of a heterochromatin protein gene the X chromosome.Mamm Genome. 1992;2(1):72-5. doi: 10.1007/BF00570443. Mamm Genome. 1992. PMID: 1543904
-
Long nonoding RNAs in the X-inactivation center.Chromosome Res. 2013 Dec;21(6-7):601-614. doi: 10.1007/s10577-013-9396-2. Chromosome Res. 2013. PMID: 24297756 Free PMC article. Review.
-
Parental imprinting studied by allele-specific primer extension after PCR: paternal X chromosome-linked genes are transcribed prior to preferential paternal X chromosome inactivation.Proc Natl Acad Sci U S A. 1992 Nov 1;89(21):10469-73. doi: 10.1073/pnas.89.21.10469. Proc Natl Acad Sci U S A. 1992. PMID: 1279680 Free PMC article.
-
Mouse X chromosome.Mamm Genome. 1991;1 Spec No:S318-31. doi: 10.1007/BF00656501. Mamm Genome. 1991. PMID: 1799807 Review. No abstract available.
Publication types
MeSH terms
LinkOut - more resources
Molecular Biology Databases
Miscellaneous