Chapelin C, Duriez B, Magnino F, Goossens M, Escudier E, Amselem S
Laboratoire de Genetique Moléculaire et Physiopathologie, Institut National de la Santé et de la Recherche Médicale (INSERM) U.468, Hôpital Henri Mondor, Créteil, France.
FEBS Lett. 1997 Jul 28;412(2):325-30. doi: 10.1016/s0014-5793(97)00800-4.
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.
动力蛋白重链(DHCs)是被称为动力蛋白的多亚基运动ATP酶复合体的主要组成部分。轴丝动力蛋白为纤毛和鞭毛的运动提供驱动力。最近的分子研究表明,多个DHC异构体由不同的基因产生。我们描述了五个人类轴丝DHC基因的分离。对人类基因组克隆的分析揭示了内含子序列的存在,这些序列被用于证明人类轴丝DHC基因位于不同的染色体上。克隆的人类DHC序列被整合到基于系统发育分析的进化方法中。组织表达研究表明,这些人类轴丝DHCs在睾丸和/或气管中表达,这两个组织具有轴丝结构,在原发性纤毛运动障碍中可能会发生改变,这使得DHC基因成为这些人类疾病发生过程中的有力候选因素。