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[小鼠植入前胚胎致密化相关基因Crg1的克隆]

[Cloning of compaction-related gene Crg1 of mouse preimplantation embryos].

作者信息

Li Wen, Lu Guang-Xiu

机构信息

Institude of Reproduction and Stem Cell Engineering, Central South University, Changsha 410078, China.

出版信息

Yi Chuan Xue Bao. 2004 Mar;31(3):246-50.

Abstract

A total of 181 8-cell embryos and 241 8-cell compacted embryos were collected respectively from C57BL/6 mouse and their cDNA was synthesized by SMART-PCR. Then PCR productions after SSH were cloned into pUCm-T vector according to the size after isolated and purified. Choice the positive clones for sequencing after being confirmed with PCR. All fragment cloned were blastered matching in GenBank for homology analysis. On the base of this work, we select two ESTs (GenBank accession No.: BQ740263 and BQ740251), which were reverse complementary to each other, assemble into a cDNA fragment, which include a whole open read frame (ORF) and submitted to GenBank with an accession number, AY134859. The target fragment were amplified from cDNA of mouse compacted embryos using primers designed according to the ORF and cloned into pUCm-T vector and sequenced. It's confirmed that the gene, Crg1, was the same as AY134859. Crg1 were also blastered matching in GenBank for homology analysis and mapped by database analyses. RT-PCR analysis of Crg1 were done in series mouse embryos, mouse embryo stem cell and mouse embryo fibroblast. We analyzed the expression of Crg1 in 8-cell embryos and 8-cell compacted embryos using semi-quantity RT-PCR. Northern-blot analysis of Crg1 expression in some adult mouse tissues was done too. The results showed that the length of Crg1 is 810 bp. It include only one exon and code a 150 amino acid protein with a theoretical molecular weight of 17670.34 Dalton. The protein is similar to a protein encoded by a known gene, Stella. Crg1 was mapped to chromosome 14 by database analyses. RT-PCR analysis shows that Crg1 expressed in series mouse embryos (2-cell embryos, 4-cell embryos, 8-cell embryos, compacted embryos and blastocyst), and expressed little higher in compacted embryos. Crg1 also expressed in mouse embryo stem cell but not expressed in mouse embryo fibroblast. The gene only expressed weakly in adult mouse ovary, but not expressed in other adult mouse tissues (brain, spleen, heart, skeletal muscle, kidney, testis, epididymis, liver and lung). So, Crg1 may related to compaction in compacted embryos and maintaining cell's pluripotentiality.

摘要

分别从C57BL/6小鼠中收集了181个8细胞胚胎和241个8细胞致密化胚胎,并通过SMART-PCR合成了它们的cDNA。然后,将SSH后的PCR产物根据分离纯化后的大小克隆到pUCm-T载体中。经PCR确认后,选择阳性克隆进行测序。对所有克隆片段在GenBank中进行比对以进行同源性分析。在此基础上,我们选择了两个彼此反向互补的EST(GenBank登录号:BQ740263和BQ740251),将它们组装成一个包含完整开放阅读框(ORF)的cDNA片段,并以登录号AY134859提交到GenBank。根据该ORF设计引物,从小鼠致密化胚胎的cDNA中扩增目标片段,克隆到pUCm-T载体中并测序。证实该基因Crg1与AY134859相同。Crg1也在GenBank中进行比对以进行同源性分析,并通过数据库分析进行定位。在系列小鼠胚胎、小鼠胚胎干细胞和小鼠胚胎成纤维细胞中进行了Crg1的RT-PCR分析。我们使用半定量RT-PCR分析了Crg1在8细胞胚胎和8细胞致密化胚胎中的表达。还进行了Crg1在一些成年小鼠组织中表达的Northern杂交分析。结果表明,Crg1的长度为810 bp。它仅包含一个外显子,编码一个150个氨基酸的蛋白质,理论分子量为17670.34道尔顿。该蛋白质与一个已知基因Stella编码的蛋白质相似。通过数据库分析,Crg1被定位到14号染色体。RT-PCR分析表明,Crg1在系列小鼠胚胎(2细胞胚胎、4细胞胚胎、8细胞胚胎、致密化胚胎和囊胚)中表达,在致密化胚胎中表达略高。Crg1也在小鼠胚胎干细胞中表达,但在小鼠胚胎成纤维细胞中不表达。该基因在成年小鼠卵巢中仅微弱表达,但在其他成年小鼠组织(脑、脾、心、骨骼肌、肾、睾丸、附睾、肝和肺)中不表达。因此,Crg1可能与致密化胚胎中的致密化过程以及维持细胞的多能性有关。

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