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人类c-kit基因的基因组组织:III类受体酪氨酸激酶的进化

Genomic organization of the human c-kit gene: evolution of the receptor tyrosine kinase subclass III.

作者信息

André C, Martin E, Cornu F, Hu W X, Wang X P, Galibert F

机构信息

Laboratoire d'Hématologie Expérimentale (CNRS-UPR no. 41), Hôpital Saint-Louis, Paris, France.

出版信息

Oncogene. 1992 Apr;7(4):685-91.

PMID:1373482
Abstract

The c-kit proto-oncogene encodes a transmembrane tyrosine kinase receptor. It belongs to receptor tyrosine kinase subclass III, which also includes the colony-stimulating factor I receptor (c-fms), platelet-derived growth factor receptors A and B (PDGFRA and PDGFRB), as well as FLT1 and FLT3/FLK2. c-kit and PDGFRA, c-fms and PDGFRB, FLT1 and FLT3/FLK2 are grouped by pair in three clusters in man on chromosome 4 band q11-q13, chromosome 5 band q31-q33 and chromosome 13 band q12 respectively. Here, we report the genomic organization of the human c-kit gene, which is composed of 21 small coding exons, distributed over 80 kb. Comparison of the c-kit and c-fms oncogenes shows that they share identified exon/intron boundaries in their two kinase domains, as well as a similar exon/intron organization in the extracytoplasmic domain. Comparison with the kinase domains of tyrosine kinase genes not belonging to subclass III suggests that the exon/intron organization of c-kit and c-fms is a characteristic feature of subclass III. The genomic similarities between c-kit and c-fms, in conjunction with the location in pairs on different chromosomes of the subclass III genes, has led us to hypothesize that cis and trans duplications gave rise to this group of genes.

摘要

c-kit原癌基因编码一种跨膜酪氨酸激酶受体。它属于III类受体酪氨酸激酶亚类,该亚类还包括集落刺激因子I受体(c-fms)、血小板衍生生长因子受体A和B(PDGFRA和PDGFRB)以及FLT1和FLT3/FLK2。在人类中,c-kit与PDGFRA、c-fms与PDGFRB、FLT1与FLT3/FLK2分别在4号染色体q11-q13带、5号染色体q31-q33带和13号染色体q12带上以两两成簇的形式排列。在此,我们报道人类c-kit基因的基因组结构,它由21个小编码外显子组成,分布在80 kb范围内。c-kit和c-fms原癌基因的比较表明,它们在两个激酶结构域中共享已确定的外显子/内含子边界,并且在胞外结构域中具有相似的外显子/内含子组织。与不属于III类的酪氨酸激酶基因的激酶结构域进行比较表明,c-kit和c-fms的外显子/内含子组织是III类的特征性特征。c-kit和c-fms之间的基因组相似性,以及III类基因在不同染色体上的成对定位,使我们推测顺式和反式复制产生了这一组基因。

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