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PCR 扩增的小鼠胚胎 cDNA 文库的差异筛选:葡萄糖转运蛋白在植入后早期小鼠胚胎中差异表达。

Differential screening of a PCR-generated mouse embryo cDNA library: glucose transporters are differentially expressed in early postimplantation mouse embryos.

作者信息

Smith D E, Gridley T

机构信息

Department of Cell and Developmental Biology, Roche Research Center, Nutley, NJ 07110.

出版信息

Development. 1992 Nov;116(3):555-61. doi: 10.1242/dev.116.3.555.

Abstract

Differential screening of a cDNA library constructed using PCR amplification techniques from RNA isolated from the distal portion (embryonic ectoderm, mesoderm and visceral endoderm) of 7.5 days post coitum (dpc) mouse embryos led to the isolation of two cDNA clones expressed at higher levels in 7.5 dpc embryos than 12.5 dpc embryos. Nucleotide sequence analysis revealed that each of these clones was a different member of the family of facilitative glucose transporters (Glut genes). The differentially expressed cDNA clones represent mouse Glut-1 and Glut-3. Levels of the Glut-3 mRNA declined 14-fold between days 7.5 and 12.5 of gestation, and were under our limits of detection by 14.5 dpc. The levels of the Glut-1 mRNA declined about 3-fold between days 7.5 and 12.5 of gestation. Analysis of the expression of these genes by in situ hybridization revealed striking differences in transcript localization in early postimplantation mouse embryos. At 7.5 dpc, both transporters were expressed more strongly in extraembryonic tissues than in the embryo proper. While both transporters were expressed in the amnion and chorion, only Glut-1 was expressed in the ectoplacental cone. In the yolk sac, Glut-3 appeared to be expressed only in the endoderm while Glut-1, although expressed in both layers, was expressed more strongly in the mesoderm layer. Thus, the two transporters have relatively reciprocal sites of expression in the developing extraembryonic membranes. Expression of Glut-1 was fairly widespread in the embryo at 8.5 dpc, but by 10.5 dpc expression was down-regulated and was observed in the eye and the spinal cord.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用聚合酶链反应(PCR)扩增技术,从交配后7.5天(dpc)小鼠胚胎远端部分(胚胎外胚层、中胚层和脏内胚层)分离的RNA构建cDNA文库,并进行差异筛选,结果分离出两个在7.5 dpc胚胎中表达水平高于12.5 dpc胚胎的cDNA克隆。核苷酸序列分析表明,这些克隆中的每一个都是易化葡萄糖转运蛋白家族(Glut基因)的不同成员。差异表达的cDNA克隆代表小鼠Glut-1和Glut-3。Glut-3 mRNA水平在妊娠7.5天至12.5天之间下降了14倍,到14.5 dpc时低于我们的检测限。Glut-1 mRNA水平在妊娠7.5天至12.5天之间下降了约3倍。通过原位杂交分析这些基因的表达,发现在植入后早期小鼠胚胎中转录本定位存在显著差异。在7.5 dpc时,两种转运蛋白在胚胎外组织中的表达均强于胚胎本身。虽然两种转运蛋白都在羊膜和绒毛膜中表达,但只有Glut-1在外胎盘圆锥中表达。在卵黄囊中,Glut-3似乎仅在内胚层中表达,而Glut-1虽然在两层中都有表达,但在中胚层中表达更强。因此,这两种转运蛋白在发育中的胚胎外膜中有相对互补的表达位点。Glut-1在8.5 dpc时在胚胎中的表达相当广泛,但到10.5 dpc时表达下调,仅在眼睛和脊髓中观察到。(摘要截短于250字)

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