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Structural organization and transcription of the mouse gastric H+, K(+)-ATPase beta subunit gene.

作者信息

Canfield V A, Levenson R

机构信息

Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06510.

出版信息

Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):8247-51. doi: 10.1073/pnas.88.18.8247.

Abstract

We have cloned and characterized the mouse gene encoding the beta subunit of H+, K(+)-ATPase (EC 3.6.1.36). The entire 10.5-kilobase transcription unit of the H+,K(+)-ATPase beta subunit gene was cloned in three overlapping cosmids encompassing approximately 46 kilobases of genomic DNA. A tight cluster of transcription initiation sites has been localized 24-25 nucleotides upstream of the translation start site and 28-29 nucleotides downstream of a TATA-like sequence. The H+, K(+)-ATPase beta subunit gene is split into seven exons encoding predicted structural domains of the beta subunit protein. The intracellular amino-terminal and putative transmembrane domains are encoded by individual exons, and the extracellular carboxyl-terminal domain is encoded by five exons. The exon/intron organization of the mouse H+,K(+)-ATPase beta subunit gene is identical to that of the mouse Na+,K(+)-ATPase beta 2 subunit gene. The conservation of genomic organization, together with the high sequence homology, indicates that the mouse H+,K(+)-ATPase beta and Na+,K(+)-ATPase beta 2 subunit genes originated from a common ancestral gene.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95ba/52484/7b0e2795dc8e/pnas01068-0356-a.jpg

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