CDNA SEQUENCE, GENE SEQUENCE, AND PROPERTIES OF MURINE PALLIDIN (BAND-4.2), THE PROTEIN IMPLICATED IN THE MURINE PALLID MUTATION

被引:18
作者
KORSGREN, C
COHEN, CM
机构
[1] ST ELIZABETHS MED CTR,DEPT BIOMED RES,BOSTON,MA 02135
[2] TUFTS UNIV,SCH MED,DEPT MED,BOSTON,MA 02111
[3] TUFTS UNIV,SCH MED,DEPT ANAT & CELLULAR BIOL,BOSTON,MA 02111
关键词
D O I
10.1006/geno.1994.1304
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Band 4.2, which plays an important but poorly understood role in erythrocyte function and survival, is a major component of erythrocyte membranes. Recently, it has been shown that the gene for murine protein band 4.2 colocalizes on chromosome 2 with the murine pallid mutation, which affects the formation or function of intracellular storage granules in melanocytes and platelets and lysosomes in kidney. As a first step in identifying the mutation responsible for the pallid phenotype, we have sequenced the entire normal murine band 4.2 gene. Our results show that the gene for murine band 4.2 is approximately 22 kb in size, with 13 exons and 12 intervening introns. The organization of the mouse band 4.2 gene is identical to that of the human band 4.2 gene and similar to that of the genes for the transglutaminase enzymes, reiterating the membership of protein band 4.2 in the transglutaminase gene superfamily. We also present 3.5 kb of normal murine erythroid band 4.2 cDNA sequence containing an open reading frame of 2073 bp and coding for 691 amino acids. This is the same size as the human erythrocyte protein, with which the murine protein shares a 72% amino acid identity. (C) 1994 Academic Press, Inc.
引用
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页码:478 / 485
页数:8
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