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一种新型小鼠ABC转运蛋白Abca13的分子结构与特性

Molecular structure and characterization of a novel murine ABC transporter, Abca13.

作者信息

Barros Scott A, Tennant Raymond W, Cannon Ronald E

机构信息

Curriculum in Toxicology, University of North Carolina at Chapel Hill, 27514, USA.

出版信息

Gene. 2003 Mar 27;307:191-200. doi: 10.1016/s0378-1119(03)00465-7.

Abstract

We report the isolation and structural characterization of the full-length gene and cDNA for a novel mouse ATP-binding cassette (ABC) transporter, Abca13. The mRNA, isolated from mouse kidney, is 6.7 kb in size and encodes a protein consisting of 2143 amino acids with a predicted molecular weight of 240 kDa. The Abca13 gene consists of 44 exons which span 360 kb of genomic sequence. Abca13 has been mapped to mouse chromosome 11.a2, revealing the human orthologue highly conserved on a syntenic region of human chromosome 7p12. The deduced mouse Abca13 protein shows highest amino acid sequence homology to human ABCA1 (50%), ABCA4 (50%), and ABCA12 (56%). Analysis of the putative Abca13 promoter region revealed potential transcription factor binding sites associated with myeloid- and lymphoid-derived cell types. mRNA transcript levels were highest in mouse submaxillary gland, epididymus, ovary, and thymus; with lower levels in a variety of other tissues. An alternative transcript was discovered in mouse kidney devoid of exon 11. The removal of exon 11 by post-transcriptional splicing causes a frameshift in the open reading frame and results in a premature termination codon. We hypothesize that the excision of exon 11 may serve as a regulatory mechanism in kidney, and perhaps other tissues as well. The molecular characterization of the mouse Abca13 gene will establish the foundation for future functional studies of the human ABCA13 transporter.

摘要

我们报道了一种新型小鼠ATP结合盒(ABC)转运蛋白Abca13全长基因及cDNA的分离和结构表征。从小鼠肾脏分离的mRNA大小为6.7 kb,编码一种由2143个氨基酸组成的蛋白质,预测分子量为240 kDa。Abca13基因由44个外显子组成,跨越360 kb的基因组序列。Abca13已被定位到小鼠染色体11.a2,揭示其人类同源物在人类染色体7p12的同线区域高度保守。推导的小鼠Abca13蛋白与人类ABCA1(50%)、ABCA4(50%)和ABCA12(56%)显示出最高的氨基酸序列同源性。对推定的Abca13启动子区域的分析揭示了与髓系和淋巴系来源细胞类型相关的潜在转录因子结合位点。mRNA转录水平在小鼠下颌下腺、附睾、卵巢和胸腺中最高;在其他多种组织中水平较低。在小鼠肾脏中发现了一种缺失外显子11的可变转录本。转录后剪接去除外显子11会导致开放阅读框移码并产生提前终止密码子。我们推测外显子11的切除可能是肾脏以及其他组织中的一种调节机制。小鼠Abca13基因的分子表征将为未来人类ABCA13转运蛋白的功能研究奠定基础。

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