Isolation of several human axonemal dynein heavy chain genes: genomic structure of the catalytic site, phylogenetic analysis and chromosomal assignment

被引:48
作者
Chapelin, C
Duriez, B
Magnino, F
Goossens, M
Escudier, E
Amselem, S
机构
[1] CHU PITIE SALPETRIERE,SERV HISTOL EMBRYOL,F-75651 PARIS 13,FRANCE
[2] HOP HENRI MONDOR,INSERM,U468,LAB GENET MOL & PHYSIOPATHOL,F-94010 CRETEIL,FRANCE
关键词
dynein; cilium; phylogeny; primary ciliary dyskinesia; human genomic DNA;
D O I
10.1016/S0014-5793(97)00800-4
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
Dynein heavy chains (DHCs) are the main components of multisubunit motor ATPase complexes called dyneins, Axonemal dyneins provide the driving force for ciliary and flagellar motility. Recent molecular studies demonstrated that multiple DHC isoforms are produced by separate genes. We describe the isolation of five human axonemal DHC genes. Analysis of the human genomic clones revealed the existence of intronic sequences that were used to demonstrate that human axonemal DHC genes are located on different chromosomes, The cloned human DHC sequences were integrated into an evolutionary approach based on phylogenetic analysis. Tissue expression studies showed that these human axonemal DHCs are expressed in testis and/or trachea, two tissues with axonemal structures that can be altered in primary ciliary dyskinesia, making DHC genes strong candidates in the genesis of these human diseases. (C) 1997 Federation of European Biochemical Societies.
引用
收藏
页码:325 / 330
页数:6
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