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几种人类动力蛋白重链基因的鉴定、组织特异性表达及染色体定位。

Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes.

作者信息

Maiti A K, Mattéi M G, Jorissen M, Volz A, Zeigler A, Bouvagnet P

机构信息

Division of Medical Genetics, Geneva University School of Medicine, Switzerland.

出版信息

Eur J Hum Genet. 2000 Dec;8(12):923-32. doi: 10.1038/sj.ejhg.5200555.

Abstract

Sliding between adjacent microtubules within the axonema gives rise to the motility of cilia and flagella. The driving force is produced by dynein complexes which are mainly composed of the axonemal dynein heavy chains. We used cells of human respiratory epithelium after in vitro ciliogenesis to clone cDNA fragments of nine dynein heavy chain genes, one of which had never been identified before. Dynein heavy chains are highly conserved from protozoa to human and the evolutionary ancestry of these dynein heavy chain cDNA fragments was deduced by phylogenetic analysis. These dynein heavy chain cDNAs are highly transcribed in human tissues containing axonema such as trachea, testis and brain, but not in adult heart or placenta. PAC clones containing dynein heavy chains were obtained and used to determine by FISH their chromosomal position in the human genome. They were mapped to 2p12-p11, 2q33, 3p21.2-p21.1, 13q14, 16p12 and 17p12. The chromosomal assignment of these dynein heavy chain genes which was confirmed by GeneBridge 4 radiation hybrid screening, will be extremely useful for linkage analysis efforts in patients with primary ciliary dyskinesia (PCD).

摘要

轴丝中相邻微管之间的滑动产生了纤毛和鞭毛的运动。驱动力由动力蛋白复合体产生,该复合体主要由轴丝动力蛋白重链组成。我们利用体外纤毛发生后的人呼吸道上皮细胞克隆了9个动力蛋白重链基因的cDNA片段,其中一个此前从未被鉴定过。从原生动物到人类,动力蛋白重链高度保守,通过系统发育分析推断出这些动力蛋白重链cDNA片段的进化谱系。这些动力蛋白重链cDNA在含有轴丝的人体组织如气管、睾丸和大脑中高度转录,但在成人心脏或胎盘中不转录。获得了包含动力蛋白重链的PAC克隆,并通过荧光原位杂交确定它们在人类基因组中的染色体位置。它们被定位到2p12 - p11、2q33、3p21.2 - p21.1、13q14、16p12和17p12。这些动力蛋白重链基因的染色体定位经基因桥4辐射杂种筛选得到证实,这对于原发性纤毛运动障碍(PCD)患者的连锁分析将极为有用。

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