Cocchia M, Huber R, Pantano S, Chen E Y, Ma P, Forabosco A, Ko M S, Schlessinger D
Laboratory of Genetics, National Institute on Aging, 5600 Nathan Shock Drive, Baltimore, Maryland 21224, USA.
Genomics. 2000 Sep 15;68(3):305-12. doi: 10.1006/geno.2000.6302.
A novel human X-linked gene shows placenta-specific expression and has been named PLAC1. The gene maps 65 kb telomeric to HPRT at Xq26 and has been completely sequenced at the cDNA and genomic levels. The mouse orthologue Plac1 maps to the syntenically equivalent region of the mouse X chromosome. In situ hybridization studies with the antisense mRNA during mouse embryogenesis detect Plac1 expression from 7.5 dpc (days postcoitum) to 14.5 dpc in ectoplacental cone, giant cells, and labyrinthine trophoblasts. The putative human and murine PLAC1 proteins are 60% identical and 77% homologous. Both include a signal peptide and a peptide sequence also found in an interaction domain of the ZP3 (zona pellucida 3) protein. These results make PLAC1 a marker for placental development, with a possible role in the establishment of the mother-fetus interface.
一个新的人类X连锁基因表现出胎盘特异性表达,已被命名为PLAC1。该基因定位于Xq26上距HPRT端粒65 kb处,并且已在cDNA和基因组水平上完成全序列测定。小鼠同源基因Plac1定位于小鼠X染色体的同线等效区域。在小鼠胚胎发育过程中用反义mRNA进行原位杂交研究,检测到Plac1在7.5 dpc(交配后天数)至14.5 dpc期间在外胎盘锥、巨细胞和迷路滋养层中表达。推测的人类和小鼠PLAC1蛋白有60%相同,77%同源。两者都包含一个信号肽和一个也存在于ZP3(透明带3)蛋白相互作用结构域中的肽序列。这些结果使PLAC1成为胎盘发育的一个标志物,可能在母胎界面的建立中起作用。