cDNA cloning and distribution of the Xenopus follistatin-related protein

被引:30
|
作者
Okabayashi, K
Shoji, H
Onuma, Y
Nakamura, T
Nose, K
Sugino, H
Asashima, M [1 ]
机构
[1] Univ Tokyo, Dept Life Sci, Meguro Ku, Tokyo 1538902, Japan
[2] Univ Tokyo, CREST Project, Meguro Ku, Tokyo 1538902, Japan
[3] Univ Tokushima, Inst Enzyme Res, Tokushima 7708053, Japan
[4] Showa Univ, Sch Pharmaceut Sci, Dept Microbiol, Shinagawa Ku, Tokyo 1420064, Japan
关键词
D O I
10.1006/bbrc.1998.9892
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recently, several proteins which have a follistatin module have been isolated. One of them, the follistatin-related protein (FRP), is encoded by TSC-36 (TGF-beta-stimulated clone 36) in mouse, originally isolated as a cDNA clone up-regulated by TGF-beta 1 in mouse osteogenic MC3T3E1 cells. To determine the physiological role of FRP in early Xenopus embryonic development, we cloned the Xenopus FRP (xFRP) cDNA The resulting cDNA clone was a secreted glycoprotein consisting of 299 amino acid residues with about 70% similarity to the mammalian and avian FRPs, Northern blotting analysis revealed that xFRP gene expression started at stage 10, the onset of gastrulation, gradually increased during the blastula and neurula stages and was sustained through the tail-bud stage. Whole-mount in situ hybridization analysis showed the localization of xFRP mRNAs in the Spemann organizer, notochord, neural floor plate, hypo-chord and somite. The similarities with the pattern of expression of Xenopus follistatin mRNA suggests that xFRP may play a role in neuralization. (C) 1999 Academic Press.
引用
收藏
页码:42 / 48
页数:7
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