Galaviz-Hernandez Carlos, Stagg Carole, de Ridder Gustaaf, Tanaka Tetsuya S, Ko Minoru S H, Schlessinger David, Nagaraja Ramaiah
Laboratory of Genetics, National Institute on Aging, NIH, Suite 3000, 333 Cassell Drive, Baltimore, MD 21224, USA.
Gene. 2003 May 8;309(2):81-9. doi: 10.1016/s0378-1119(03)00508-0.
Microarray expression profiling of a collection of 15,000 mouse genes with placental and embryonic RNAs revealed candidates for placental-enriched genes, three of which we have confirmed and further characterized. One, Plac1, strongly expressed in all trophoblast-derived cells in the placenta, has been described earlier (Genomics 68 (2000) 305). Here we report that of the other two, Plac8 expression is restricted to the spongiotrophoblast layer during development, whereas Plac9 is weakly expressed though highly enriched in placenta. For both, cDNAs with complete open reading frames were recovered and exon-intron structures inferred from comparisons of mouse cDNA and genomic sequence. The predicted proteins (112 and 108 amino acids) both contain putative signal peptides, with a coiled-coil segment of mPLAC9 as the only other detected motif. Genomic sequence comparisons reveal that in addition to an apparent pseudogene on chromosome 1, Plac8 is expressed at mouse cytoband 5e3. It is tightly conserved in human in a syntenically equivalent ortholog at 4q21.23. Plac9 is present in a single copy on chromosome 14, with a syntenically equivalent human ortholog at 10q22.3. Putative promoter regions up to 10 kb 5' of the transcription units for Plac1, Plac8, and Plac9 contain sites for widely-expressed transcription factors which, by analogy to other instances, may be sufficient to explain placental enrichment.
利用胎盘和胚胎RNA对15000个小鼠基因进行微阵列表达谱分析,发现了胎盘富集基因的候选基因,其中三个已得到证实并作了进一步表征。其中一个基因Plac1,在胎盘中所有滋养层来源的细胞中均强烈表达,此前已有描述(《基因组学》68卷(2000年)第305页)。在此我们报告,另外两个基因中,Plac8的表达在发育过程中局限于海绵滋养层,而Plac9虽在胎盘中高度富集但表达较弱。对于这两个基因,均获得了具有完整开放阅读框的cDNA,并通过比较小鼠cDNA和基因组序列推断出其外显子-内含子结构。预测的蛋白质(分别为112和108个氨基酸)均含有假定的信号肽,mPLAC9的卷曲螺旋区段是唯一检测到的其他基序。基因组序列比较显示,除了1号染色体上一个明显的假基因外,Plac8在小鼠细胞带5e3处表达。它在人类中与4q21.23处的同线性等效直系同源基因紧密保守。Plac9在14号染色体上以单拷贝形式存在,在人类中与10q22.3处的同线性等效直系同源基因对应。Plac1、Plac8和Plac9转录单元5'端上游长达10 kb的假定启动子区域含有广泛表达的转录因子的位点,类比其他情况,这些位点可能足以解释其在胎盘中的富集。