Sanford L P, Ormsby I, Gittenberger-de Groot A C, Sariola H, Friedman R, Boivin G P, Cardell E L, Doetschman T
Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati, OH 45267, USA.
Development. 1997 Jul;124(13):2659-70. doi: 10.1242/dev.124.13.2659.
The growth and differentiation factor transforming growth factor-beta2 (TGFbeta2) is thought to play important roles in multiple developmental processes. Targeted disruption of the TGFbeta2 gene was undertaken to determine its essential role in vivo. TGFbeta2-null mice exhibit perinatal mortality and a wide range of developmental defects for a single gene disruption. These include cardiac, lung, craniofacial, limb, spinal column, eye, inner ear and urogenital defects. The developmental processes most commonly involved in the affected tissues include epithelial-mesenchymal interactions, cell growth, extracellular matrix production and tissue remodeling. In addition, many affected tissues have neural crest-derived components and simulate neural crest deficiencies. There is no phenotypic overlap with TGFbeta1- and TGFbeta3-null mice indicating numerous non-compensated functions between the TGFbeta isoforms.
生长与分化因子转化生长因子-β2(TGFβ2)被认为在多个发育过程中发挥重要作用。为了确定其在体内的关键作用,对TGFβ2基因进行了靶向破坏。TGFβ2基因缺失的小鼠表现出围产期死亡率以及单一基因破坏所导致的广泛发育缺陷。这些缺陷包括心脏、肺、颅面、肢体、脊柱、眼睛、内耳和泌尿生殖系统缺陷。受影响组织中最常涉及的发育过程包括上皮-间充质相互作用、细胞生长、细胞外基质产生和组织重塑。此外,许多受影响的组织具有神经嵴衍生成分,并模拟神经嵴缺陷。与TGFβ1和TGFβ3基因缺失的小鼠没有表型重叠,这表明TGFβ亚型之间存在许多非补偿性功能。