Identification of four trp1 gene variants murine pancreatic beta-cells

被引:63
作者
Sakura, H [1 ]
Ashcroft, FM [1 ]
机构
[1] UNIV OXFORD,PHYSIOL LAB,OXFORD OX1 3PT,ENGLAND
基金
英国惠康基金;
关键词
trp1; Ca-release activated channel; pancreatic beta cell; MIN6; cell; insulin secretion;
D O I
10.1007/s001250050711
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin secretion is stimulated by glucose, hormones and neurotransmitters. Both activation of a non-selective cation current and activation of a Ca2+ current in response to depletion of intracellular Ca2+ stores have been suggested to play a role in this stimulation, The properties of these currents resemble those reported for the Drosophila genes trp and trpl. Using the reverse transcription polymerase chain reaction and Northern blot analysis we found that of the six mammalian trp-related genes (trp1-6), only trp1 was expressed at high levels in the mouse insulinoma cell line MING. We cloned the murine homologue of human trp1 from MING cells and identified four variants (alpha, beta, gamma and delta), generated by alternative splicing near the N-terminus of the protein. In vitro translation showed that only the alpha and beta splice variants are efficiently expressed. The beta variant is the dominant form in MIN6 cells (and probably in mouse pancreatic islets), whereas the alpha variant is the major type in the mouse brain. The beta variant showed 99% identity to the human homologue at the amino acid level.
引用
收藏
页码:528 / 532
页数:5
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