Literature DB >> 2209467

Molecular analysis of the Mov 34 mutation: transcript disrupted by proviral integration in mice is conserved in Drosophila.

T Gridley1, D A Gray, T Orr-Weaver, P Soriano, D E Barton, U Francke, R Jaenisch.   

Abstract

The Mov 34 mutation is a recessive embryonic lethal mutation caused by retroviral integration in the murine germline. This integration disrupts a transcription unit that appears to encode a novel protein. The Mov 34 proviral integration is located on mouse chromosome 8 and the human homolog of this gene has been mapped to chromosome region 16q23-q24. An evolutionarily conserved syntenic relationship exists between this region of human chromosome 16 and a region of mouse chromosome 8 that also contains oligosyndactyly (Os), another recessive lethal mutation. Genetic studies have ruled out Os as residing at the same locus as the Mov 34 integration. The Mov 34 transcript is conserved in evolution, and a Drosophila homolog appears to encode a protein with 62% amino acid identity to the murine protein. In situ hybridization to Drosophila polytene chromosomes localizes the Drosophila homolog to 60B,C on chromosome 2. Several Drosophila lethal mutations also map to this region.

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Year:  1990        PMID: 2209467     DOI: 10.1242/dev.109.1.235

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  11 in total

Review 1.  Mouse chromosome 8.

Authors:  J D Ceci; A J Lusis
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Mouse chromosome 8.

Authors:  J D Ceci
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-07-25       Impact factor: 16.971

4.  High-resolution mapping of a linkage group on mouse chromosome 8 conserved on human chromosome 16Q.

Authors:  J Becker-Follmann; A Gaa; E Baùsch; E Natt; G Scherer; O von Deimling
Journal:  Mamm Genome       Date:  1997-03       Impact factor: 2.957

5.  Proviral inactivation of the Npat gene of Mpv 20 mice results in early embryonic arrest.

Authors:  M Di Fruscio; H Weiher; B C Vanderhyden; T Imai; T Shiomi; T A Hori; R Jaenisch; D A Gray
Journal:  Mol Cell Biol       Date:  1997-07       Impact factor: 4.272

Review 6.  Subunits of the regulatory complex of the 26S protease.

Authors:  W Dubiel; K Ferrell; M Rechsteiner
Journal:  Mol Biol Rep       Date:  1995       Impact factor: 2.316

7.  Mov34 protein from mouse brain interacts with the 3' noncoding region of Japanese encephalitis virus.

Authors:  M Ta; S Vrati
Journal:  J Virol       Date:  2000-06       Impact factor: 5.103

8.  CDNA cloning of p112, the largest regulatory subunit of the human 26s proteasome, and functional analysis of its yeast homologue, sen3p.

Authors:  K Yokota; S Kagawa; Y Shimizu; H Akioka; C Tsurumi; C Noda; M Fujimuro; H Yokosawa; T Fujiwara; E Takahashi; M Ohba; M Yamasaki; G N DeMartino; C A Slaughter; A Toh-e; K Tanaka
Journal:  Mol Biol Cell       Date:  1996-06       Impact factor: 4.138

9.  Interaction between proliferating cell nuclear antigen and JUN-activation-domain-binding protein 1 in the meristem of rice, Oryza sativa L.

Authors:  Taichi Yamamoto; Seisuke Kimura; Yoko Mori; Yukinobu Uchiyama; Toyotaka Ishibashi; Junji Hashimoto; Kengo Sakaguchi
Journal:  Planta       Date:  2003-03-15       Impact factor: 4.116

Review 10.  Insertional mutagenesis in transgenic mice.

Authors:  T Rijkers; A Peetz; U Rüther
Journal:  Transgenic Res       Date:  1994-07       Impact factor: 2.788

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