Monstein H J, Nilsson I, Ellnebo-Svedlund K, Svensson S P
Division of Clinical Microbiology, Molecular Biology Laboratory, LMO, University Hospital, Linköping, Sweden.
Recept Channels. 1998;6(3):165-77.
We report here the cloning and characterization of a 5'-end alternatively spliced human cholecystokinin-B (CCK-B) receptor mRNA. The 5'-end of this CCK-B receptor transcript (termed CCK-BRtx) consisted of exon Ia, present in the ordinary full-length CCK-B receptor mRNA (CCK-BRwt), and exon Ib, present in a previously described 5'-end alternatively spliced CCK-B receptor mRNA (CCK-BRt). A short open reading frame preceded the AUG translation initiation codon of the CCK-BRtx. Transfection of COS-7 cells with the CCK-BRtx or CCK-BRt cDNAs did not lead to the appearance of peptidergic and non-peptidergic binding sites. Cell free in vitro translation yielded proteins of approximately 44 kDa (CCK-B receptor) and 40 kDa (CCK-BRt receptor) whereas no 40 kDa product was detected from the cloned CCK-BRtx cDNA. Instead, a protein product of approximately 9 kDa was visualized, the size corresponding to the predicted protein encoded by the short open reading frame. The alternatively spliced CCK-B receptor transcripts were concomitantly expressed with the ordinary full-length CCK-B receptor mRNA in the brain, pancreas, and stomach. The possibility that such transcripts are translated in vivo into truncated CCK-B receptors is discussed.
我们在此报告一种5'-末端可变剪接的人胆囊收缩素B(CCK-B)受体mRNA的克隆及特性。该CCK-B受体转录本(称为CCK-BRtx)的5'-末端由普通全长CCK-B受体mRNA(CCK-BRwt)中存在的外显子Ia和先前描述的5'-末端可变剪接的CCK-B受体mRNA(CCK-BRt)中存在的外显子Ib组成。在CCK-BRtx的AUG翻译起始密码子之前有一个短开放阅读框。用CCK-BRtx或CCK-BRt cDNA转染COS-7细胞未导致肽能和非肽能结合位点的出现。无细胞体外翻译产生了约44 kDa的蛋白质(CCK-B受体)和40 kDa的蛋白质(CCK-BRt受体),而从克隆的CCK-BRtx cDNA中未检测到40 kDa的产物。相反,观察到了一个约9 kDa的蛋白质产物,其大小与由短开放阅读框编码的预测蛋白质相对应。可变剪接的CCK-B受体转录本与普通全长CCK-B受体mRNA在脑、胰腺和胃中同时表达。本文讨论了此类转录本在体内是否会被翻译成截短的CCK-B受体的可能性。