Chan Agnes P, Kloc Malgorzata, Larabell Carolyn A, LeGros Mark, Etkin Laurence D
Department of Molecular Genetics, University of Texas, M.D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA.
Mech Dev. 2007 May;124(5):350-63. doi: 10.1016/j.mod.2007.02.001. Epub 2007 Feb 21.
Fatvg is a localized maternal transcript that translocates to the vegetal cortex of Xenopus laevis oocytes through both the METRO and Late RNA localization pathways. It is a member of a gene family that functions in vesicular trafficking. Depletion of the maternal store of fatvg mRNA results in a dual phenotype in which embryos are ventralized and also lack primordial germ cells. This complex fatvg loss of function phenotype is the result of stabilization of the dorsalizing factor beta-catenin at the vegetal pole and the inability of the germ cell determinants to move to their proper locations. This is coincident with the inhibition of cortical rotation and the abnormal aggregation of the germ plasm. Fatvg protein is located at the periphery of vesicles in the oocyte and embryo, supporting its proposed role in vesicular trafficking in the embryo. These results point to a common fundamental mechanism that is regulated by fatvg through which germ cell determinants and dorsalizing factors segregate during early development.
Fatvg是一种局部化的母源转录本,它通过METRO和晚期RNA定位途径转运到非洲爪蟾卵母细胞的植物皮质。它是一个在囊泡运输中起作用的基因家族的成员。母源fatvg mRNA储备的耗尽会导致双重表型,即胚胎腹化且缺乏原始生殖细胞。这种复杂的fatvg功能丧失表型是由于植物极的背化因子β-连环蛋白的稳定以及生殖细胞决定因子无法移动到其正确位置所致。这与皮质旋转的抑制和生殖质的异常聚集同时发生。Fatvg蛋白位于卵母细胞和胚胎中囊泡的外周,支持其在胚胎囊泡运输中的推测作用。这些结果表明存在一种由fatvg调控的共同基本机制,通过该机制生殖细胞决定因子和背化因子在早期发育过程中分离。