Hauser F, Hoffmann W
Max-Planck-Institut für Psychiatrie, Abteilung Neurochemie, Martinsried, Federal Republic of Germany.
J Biol Chem. 1991 Nov 5;266(31):21306-9.
Two different precursors for secretory polypeptides from the stomach of Xenopus laevis have been characterized by cDNA cloning. Both mature polypeptides are potential candidates for gastrointestinal growth factors. One, xP1, is the X. laevis homologue of the pS2 gene product consisting only of a single P-domain, whereas the second, xP4, is a novel polypeptide formed by four P-domains arranged in tandem. Northern analysis detected both transcripts in the stomach but not in the skin or the brain. In situ hybridizations localized the expression of both precursors in surface mucous cells of the gastric mucosa. With an antibody generated against the deduced C-terminal end of xP4, the mature polypeptide was investigated by Western analysis revealing N-glycosylation of xP4.
通过cDNA克隆对非洲爪蟾胃中分泌性多肽的两种不同前体进行了表征。两种成熟多肽都是胃肠生长因子的潜在候选物。一种是xP1,它是仅由单个P结构域组成的pS2基因产物的非洲爪蟾同源物,而另一种是xP4,它是由四个串联排列的P结构域形成的新型多肽。Northern分析在胃中检测到了这两种转录本,但在皮肤或大脑中未检测到。原位杂交将两种前体的表达定位在胃黏膜的表面黏液细胞中。利用针对xP4推导的C末端产生的抗体,通过Western分析对成熟多肽进行了研究,揭示了xP4的N-糖基化。