Literature DB >> 2076813

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

C A Howard1, G R Gummere, M F Lyon, D Bennett, K Artzt.   

Abstract

The t-complex is located on the proximal third of chromosome 17 in the house mouse. Naturally occurring variant forms of the t-complex, known as complete t-haplotypes, are found in wild mouse populations. The t-haplotypes contain at least four nonoverlapping inversions that suppress recombination with the wild-type chromosome, and lock into strong linkage disequilibrium loci affecting normal transmission of the chromosome, male gametogenesis and embryonic development. Partial t-haplotypes derived through rare recombination between t-haplotypes and wild-type homologs have been critical in the analysis of these properties. Utilizing two new DNA probes. Au3 and Au9, and several previously described probes, we have analyzed the genetic structure of several partial t-haplotypes that have arisen in our laboratory, as well as several wild-type chromosomes deleted for loci in this region. With this approach we have been able to further our understanding of the structural and dynamic characteristics of the proximal region of the t-complex. Specifically, we have localized the D17Tul locus as most proximal known in t-haplotypes, achieved a better structural analysis of the partial t-haplotype t6, and defined the structure and lethal gene content of partial t-haplotypes derived from the lethal tw73 haplotype.

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Year:  1990        PMID: 2076813      PMCID: PMC1204273     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  31 in total

1.  INVESTIGATIONS OF THE NATURE OF T-ALLELES IN THE MOUSE. I. GENETIC ANALYSIS OF A SERIES OF MUTANTS DERIVED FROM A LETHAL ALLELE.

Authors:  M F LYON; R MEREDITH
Journal:  Heredity (Edinb)       Date:  1964-05       Impact factor: 3.821

2.  Molecular cloning and genetic mapping of the t complex responder candidate gene family.

Authors:  D C Bullard; J C Schimenti
Journal:  Genetics       Date:  1990-04       Impact factor: 4.562

3.  Sequence of a cDNA coding for mouse manganese superoxide dismutase.

Authors:  R A Hallewell; G T Mullenbach; M M Stempien; G I Bell
Journal:  Nucleic Acids Res       Date:  1986-12-09       Impact factor: 16.971

4.  Five of the nine genetically defined regions of mouse t haplotypes are involved in transmission ratio distortion.

Authors:  L M Silver; D Remis
Journal:  Genet Res       Date:  1987-02       Impact factor: 1.588

5.  Genetic Change in Mutations at the T/t-Locus in the Mouse.

Authors:  D Bennett; L C Dunn; K Artzt
Journal:  Genetics       Date:  1976-06       Impact factor: 4.562

6.  The effect of experimentally induced triploidy on the lethal expression of the t(12) mutation in mouse embryos.

Authors:  J McGrath; N Hillman
Journal:  Dev Biol       Date:  1982-01       Impact factor: 3.582

7.  T(16: 17)43H translocation as a tool in analysis of the proximal part of chromosome 17 (including T-t gene complex) of the mouse.

Authors:  J Forejt; J Capková; S Gregorová
Journal:  Genet Res       Date:  1980-04       Impact factor: 1.588

8.  Molecular probes define different regions of the mouse t complex.

Authors:  H S Fox; G R Martin; M F Lyon; B Herrmann; A M Frischauf; H Lehrach; L M Silver
Journal:  Cell       Date:  1985-01       Impact factor: 41.582

9.  A diversified set of testicular cell proteins specified by genes within the mouse t complex.

Authors:  L M Silver; J Uman; J Danska; J I Garrels
Journal:  Cell       Date:  1983-11       Impact factor: 41.582

10.  Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes.

Authors:  B Herrmann; M Bućan; P E Mains; A M Frischauf; L M Silver; H Lehrach
Journal:  Cell       Date:  1986-02-14       Impact factor: 41.582

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  12 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.  Tint maps to mouse chromosome 6 and may interact with a notochordal enhancer of Brachyury.

Authors:  Jiang I Wu; M A Centilli; Gabriela Vasquez; Susan Young; Jonathan Scolnick; Larissa A Durfee; Jimmy L Spearow; Staci D Schwantz; Gabriela Rennebeck; Karen Artzt
Journal:  Genetics       Date:  2007-10       Impact factor: 4.562

Review 6.  Mouse chromosome 17.

Authors:  K Artzt; D Barlow; W F Dove; K Fischer-Lindahl; J Klein; M F Lyon; L M Silver
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

7.  The proximal end of mouse chromosome 17: new molecular markers identify a deletion associated with quakingviable.

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

8.  Targeted mutagenesis of a candidate t complex responder gene in mouse t haplotypes does not eliminate transmission ratio distortion.

Authors:  U K Ewulonu; K Schimenti; B Kuemerle; T Magnuson; J Schimenti
Journal:  Genetics       Date:  1996-10       Impact factor: 4.562

9.  The mouse plasminogen locus maps to the recombination breakpoints of the tLub2 and TtOrl partial t haplotypes but is not at the tw73 locus.

Authors:  N Schweifer; D P Barlow
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

10.  Myelin/oligodendrocyte glycoprotein is a member of a subset of the immunoglobulin superfamily encoded within the major histocompatibility complex.

Authors:  D Pham-Dinh; M G Mattei; J L Nussbaum; G Roussel; P Pontarotti; N Roeckel; I H Mather; K Artzt; K F Lindahl; A Dautigny
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-01       Impact factor: 11.205

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