Literature DB >> 6722884

Transmission ratio distortion in mouse t-haplotypes is due to multiple distorter genes acting on a responder locus.

M F Lyon.   

Abstract

Transmission ratios of male mice heterozygous for various combinations of partial t-haplotypes provide evidence in support of a model for the genetic basis of ratio distortion, involving two or more distorter genes acting on a responder locus. The t form of the responder locus, Tcr, in the medial part of the haplotype, must be present and heterozygous for distortion to occur. When the responder alone is present, as in t low haplotypes, the chromosome carrying it is transmitted in a low ratio (less than 50%). The t forms of the distorter loci act additively, in cis or trans, to raise the transmission of whichever chromosome carries Tcr. Identified distorter loci are Tcd-1, in the proximal part of the haplotype, Tcd-2, distal to Tcr, and probably Tcd-3, lying between Tcr and Tcd-2. In the absence of Tcr the distorters are transmitted normally. The system is compared with the SD system of Drosophila.

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Year:  1984        PMID: 6722884     DOI: 10.1016/0092-8674(84)90393-3

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  66 in total

1.  Physical mapping of male fertility and meiotic drive quantitative trait loci in the mouse t complex using chromosome deficiencies.

Authors:  A Planchart; Y You; J C Schimenti
Journal:  Genetics       Date:  2000-06       Impact factor: 4.562

2.  Narrowing the critical regions for mouse t complex transmission ratio distortion factors by use of deletions.

Authors:  M F Lyon; J C Schimenti; E P Evans
Journal:  Genetics       Date:  2000-06       Impact factor: 4.562

3.  New molecular markers for the distal end of the t-complex and their relationships to mutations affecting mouse development.

Authors:  T Ebersole; F Lai; K Artzt
Journal:  Genetics       Date:  1992-05       Impact factor: 4.562

Review 4.  Mouse chromosome 17.

Authors:  L M Silver; K Artzt; D Barlow; K Fischer-Lindahl; M F Lyon; J Klein; L Snyder
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

5.  Molecular organization and evolution of the D17Leh80-like loci in the mouse t complex.

Authors:  V A Filippov; E V Fedorova; I B Rogozin; N G Kholodilov; A O Ruvinsky
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

6.  Molecular organization of the D-Qa region of t-haplotypes suggests that recombination is an important mechanism for generating genetic diversity of the major histocompatibility complex.

Authors:  H Uehara; K Abe; L Flaherty; D Bennett; K Artzt
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

7.  Submegabase clusters of unstable tandem repeats unique to the Tla region of mouse t haplotypes.

Authors:  H Uehara; T Ebersole; D Bennett; K Artzt
Journal:  Genetics       Date:  1990-12       Impact factor: 4.562

8.  Genetic and molecular analysis of the proximal region of the mouse t-complex using new molecular probes and partial t-haplotypes.

Authors:  C A Howard; G R Gummere; M F Lyon; D Bennett; K Artzt
Journal:  Genetics       Date:  1990-12       Impact factor: 4.562

9.  Retention of gene products in syncytial spermatids promotes non-Mendelian inheritance as revealed by the t complex responder.

Authors:  Nathalie Véron; Hermann Bauer; Andrea Y Weisse; Gerhild Lüder; Martin Werber; Bernhard G Herrmann
Journal:  Genes Dev       Date:  2009-12-01       Impact factor: 11.361

10.  Nucleotide sequence of a mouse Tcp-1 pseudogene: a nucleotide record for a t complex gene carried by an ancestor of the mouse.

Authors:  H Kubota; T Morita; Y Satta; M Nozaki; A Matsushiro
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

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