| Literature DB >> 11944926 |
Yoo-Seok Hwang1, Jeong-Jae Seo, Sang-Wook Cha, Hyun-Shik Lee, Sung-Young Lee, Dong-Hyun Roh, Hsiang-fu Kung Hf, Jaebong Kim, Mae Ja Park.
Abstract
Xenopus homeobox gene, PV.1 ventralizes activin-induced dorsal mesoderm and inhibits neuralization of ectoderm in animal cap when overexpressed. Here we generated PV.1/engrailed fusion construct (N-PV1-EnR) to perform loss-of-function study for this transcription factor. N-PV1-EnR showed an extremely antimorphic effect, causing a partial secondary embryonic axis when expressed at ventral marginal zone of blastula. In ventral marginal zone cells, this chimeric protein induced organizer genes and suppressed ventral markers mimicking those effects reported for dominant negative BMP-4 receptor (DNBR). Moreover, N-PV1-EnR rescued the ventralized embryos caused by the ectopic dorsal expression of PV.1 but not by that of Xvent-2. These results suggested that PV.1 functions at downstream of BMP-4 as a ventralizing effector which acts separately from Xvent-2 and the dominant negative effect gained by this specific mutant is applicable for the further studies of BMP-4 downstream pathway. (c)2002 Elsevier Science (USA).Entities:
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Year: 2002 PMID: 11944926 DOI: 10.1006/bbrc.2002.6740
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575