Advances in Na+,K+‐ATPase studies: from protein to gene and back to protein

FEBS Letters

Sverdlov, E.D.¹  Modyanov, N.N.¹  Monastyrskaya, G.S.¹  Broude, N.E.¹ 

[1] Shemyakin Institute of Bioorganic Chemistry, USSR Academy of Sciences, 117871 Moscow, USSR

关键词: Na+;    K+-ATPase;    Isoform;    Gene sequence;    Exon-intron structure;    Protein spatial organization;    Gene evolution;   

DOI  :  10.1016/0014-5793(89)81773-9

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

Complete primary structures of both subunits of Na⁺,K⁺,ATPase from various sources have been established by a combination of the methods for molecular cloning and protein chemistry. The gene family homologous to the α-subunit cDNA of animal Na⁺,K⁺-ATPases has been found in the human genome. Some genes of this family encode the known isoforms (αI and αII) of the Na⁺,K⁺-ATPase catalytic subunit. The proteins coded by other genes can be either new isoforms of the Na⁺,K⁺-ATPase catalytic subunit or other ion-transporting ATPases. Expression of the genes of this family proceeds in a tissue-specific manner and changes during the postnatal development and neoplastic transformation. The complete exon-intron structure of one of the genes of this family has been established. This gene codes for the form of the catalytic subunit, the existence of which has been unknown. Apparently, all the genes of the discovered family have a similar intron-exon structure. There is certain correlation between the gene structure and the proposed domain arrangement of the α-subunit. The results obtained have become the basis for the experiments which prove the existence of the earlier unknown αIII isoform of the Na⁺,K⁺-ATPase catalytic subunit and have made possible the study of its function.

【 授权许可】

Unknown