Human and rodent MaxiK channel beta-subunit genes: Cloning and characterization

Citation
Z. Jiang et al., Human and rodent MaxiK channel beta-subunit genes: Cloning and characterization, GENOMICS, 55(1), 1999, pp. 57-67
Citations number
32
Categorie Soggetti
Molecular Biology & Genetics
Journal title
GENOMICS
ISSN journal
08887543 → ACNP
Volume
55
Issue
1
Year of publication
1999
Pages
57 - 67
Database
ISI
SICI code
0888-7543(19990101)55:1<57:HARMCB>2.0.ZU;2-4
Abstract
Voltage- and Ca2+-sensitive K+ (MaxiK) channels play hey roles in controlli ng neuronal excitability and vascular tone. We cloned and analyzed human an d rodent genes for the modulatory beta subunit, KCNMB1. The human and mouse beta-subunit genes are similar to 11 and similar to 9 kb in length, respec tively, and have a four exon-three intron structure. Primer extension assay localized the transcription initiation site at 442 (human) or 440 (mouse) bp upstream of the translation initiation codon, agreeing with the transcri pt size in Northern blots, Both genes have a TATA-less putative promoter re gion, with a transcription initiator-like region, and motifs characteristic of regulated promoters, including muscle-specific enhancing factors-1 and -2. Consistent with a tissue-specific expression of KCNMB1, regulated at th e transcriptional level, beta-subunit transcripts are abundant in smooth mu scle and heart, but scarce in lymphatic tissues, brain, and liver. Expresse d rat and mouse beta subunits increase the apparent Ca2+ sensitivity of the human MaxiK channel alpha subunit. (C) 1999 Academic Press.