Lingrel Jerry, Moseley Amy, Dostanic Iva, Cougnon Marc, He Suiwen, James Paul, Woo Alison, O'Connor Kyle, Neumann Jonathan
Department of Molecular Genetics, Biochemistry, and Microbiology, University of Cincinnati, Ohio 45267-0524, USA.
Ann N Y Acad Sci. 2003 Apr;986:354-9. doi: 10.1111/j.1749-6632.2003.tb07214.x.
The Na,K-ATPase is composed of two subunits, alpha and beta, and each subunit consists of multiple isoforms. In the case of alpha, four isoforms, alpha1, alpha2, alpha3, and alpha4 are present in mammalian cells. The distribution of these isoforms is tissue- and developmental-specific, suggesting that they may play specific roles, either during development or coupled to specific physiological processes. In order to understand the functional properties of each of these isoforms, we are using gene targeting, where animals are produced lacking either one copy or both copies of the corresponding gene or have a modified gene. To date, we have produced animals lacking the alpha1 and alpha2 isoform genes. Animals lacking both copies of the alpha1 isoform gene are not viable, while animals lacking both copies of the alpha2 isoform gene make it to birth, but are either born dead or die very soon after. In the case of animals lacking one copy of the alpha1 or alpha2 isoform gene, the animals survive and appear healthy. Heart and EDL muscle from animals lacking one copy of the alpha2 isoform exhibit an increase in force of contraction, while there is reduced force of contraction in both muscles from animals lacking one copy of the alpha1 isoform gene. These studies indicate that the alpha1 and alpha2 isoforms carry out different physiological roles. The alpha2 isoform appears to be involved in regulating Ca(2+) transients involved in muscle contraction, while the alpha1 isoform probably plays a more generalized role. While we have not yet knocked out the alpha3 or alpha4 isoform genes, studies to date indicate that the alpha4 isoform is necessary to maintain sperm motility. It is thus possible that the alpha2, alpha3, and alpha4 isoforms are involved in specialized functions of various tissues, helping to explain their tissue- and developmental-specific regulation.
钠钾ATP酶由α和β两个亚基组成,每个亚基又包含多种亚型。就α亚基而言,哺乳动物细胞中有四种亚型,即α1、α2、α3和α4。这些亚型的分布具有组织和发育特异性,这表明它们可能在发育过程中或与特定生理过程相关联时发挥特定作用。为了了解这些亚型各自的功能特性,我们正在使用基因靶向技术,即培育缺失相应基因一个拷贝或两个拷贝的动物,或者培育具有修饰基因的动物。迄今为止,我们已经培育出了缺失α1和α2亚型基因的动物。缺失α1亚型基因两个拷贝的动物无法存活,而缺失α2亚型基因两个拷贝的动物能够出生,但要么出生时就是死胎,要么出生后很快死亡。对于缺失α1或α2亚型基因一个拷贝的动物,它们能够存活且看起来健康。缺失α2亚型基因一个拷贝的动物的心脏和趾长伸肌收缩力增强,而缺失α1亚型基因一个拷贝的动物的这两种肌肉收缩力均减弱。这些研究表明,α1和α2亚型发挥着不同的生理作用。α2亚型似乎参与调节肌肉收缩过程中涉及的钙离子瞬变,而α1亚型可能发挥更广泛的作用。虽然我们尚未敲除α3或α4亚型基因,但迄今为止的研究表明,α4亚型对于维持精子活力是必需的。因此,α2、α3和α4亚型有可能参与各种组织的特殊功能,这有助于解释它们在组织和发育方面的特异性调节。