Cloning, genomic organization and chromosomal assignment of the mouse p190-B gene

被引:15
|
作者
Burbelo, PD [1 ]
Finegold, AA
Kozak, CA
Yamada, Y
Takami, H
机构
[1] Georgetown Univ, Med Ctr, Lombardi Canc Ctr, Washington, DC 20007 USA
[2] NIDR, Pain & Neurosensory Mechanisms Branch, NIH, Bethesda, MD 20892 USA
[3] NIDR, Lab Craniofacial Dev Biol, NIH, Bethesda, MD 20892 USA
[4] NIDR, Regenerat Branch, NIH, Bethesda, MD 20892 USA
[5] NIAID, Mol Microbiol Lab, NIH, Bethesda, MD 20892 USA
关键词
genomic organization; chromosomal assignment; mouse p190-B gene; cloning;
D O I
10.1016/S0167-4781(98)00207-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The p190 family of GTPases consists of at least two different isoforms both containing an N-terminal GTPase and a C-terminal Rho GAP domain. Here we have isolated and characterized genomic and cDNA clones spanning the entire coding region of the mouse p190-B gene. Genomic data were obtained by sequencing plasmid subclones of two overlapping mouse genomic phage clones. Interestingly, a single 3.9 kb exon was found to contain approx. 80% of the coding region of the mouse p190-B protein (amino acid residues 1-1238) including the 5'-untranslated region, the N-terminal GTPase domain and a middle domain of unknown function. Missing from this exon, however, was the C-terminal Rho GAP domain, which was cloned from mouse brain mRNA using reverse transcriptase polymerase chain reaction. Comparison of the mouse with the human p190-B proteins revealed that approx. 97% of the amino acid residues were identical. Northern analysis of total RNA from a variety of mouse tissues detected ubiquitous expression of two p190-B transcripts of 4.0 and 6.8 kb in size. Analysis of two multilocus genetic crosses localized the mouse gene, Gfi2, to a position on chromosome 12, consistent with the mapping of the human gene to a position of conserved synteny on chromosome 14. The high level of sequence homology between the human and the mouse suggests that there is a strong selective pressure to maintain the p190-B protein structure. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:203 / 210
页数:8
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