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缺乏含Sm基序蛋白Lsm4的小鼠在植入前致死性

Peri-implantation lethality in mice lacking the Sm motif-containing protein Lsm4.

作者信息

Hirsch E, Oohashi T, Ahmad M, Stamm S, Fässler R

机构信息

Max Planck Institut für Biochemie, 82152 Martinsried, Germany.

出版信息

Mol Cell Biol. 2000 Feb;20(3):1055-62. doi: 10.1128/MCB.20.3.1055-1062.2000.

Abstract

Small nuclear ribonucleoproteins (snRNPs) are particles present only in eukaryotic cells. They are involved in a large variety of RNA maturation processes, most notably in pre-mRNA splicing. Several of the proteins typically found in snRNPs contain a sequence signature, the Sm domain, conserved from yeast to mammals. By using a promoter trap strategy to target actively transcribed loci in murine embryonic stem cells, a new murine gene encoding an Sm motif-containing protein was identified. Database searches revealed that it is the mouse orthologue of Lsm4p, a protein found in yeast and human cells and putatively associated with U6 snRNA. Introduction of the geo reporter gene cassette under the control of the murine Lsm4 (mLsm4) endogenous promoter showed that the gene was ubiquitously transcribed in embryonic and adult tissues. The insertion of the geo cassette disrupted the mLsm4 allele, and homozygosity for the mutation led to a recessive embryonic lethal phenotype. mLsm4-null zygotes survived to the blastocyst stages, implanted into the uterus, but died shortly thereafter. The early death of mLsm4p-null mice suggests that the role of mLsm4p in splicing is essential and cannot be compensated by other Lsm proteins.

摘要

小核核糖核蛋白(snRNPs)是仅存在于真核细胞中的颗粒。它们参与多种RNA成熟过程,最显著的是在前体mRNA剪接中。通常在snRNPs中发现的几种蛋白质含有一个序列特征,即Sm结构域,从酵母到哺乳动物都保守。通过使用启动子捕获策略靶向小鼠胚胎干细胞中活跃转录的基因座,鉴定出一个编码含Sm基序蛋白的新小鼠基因。数据库搜索显示,它是Lsm4p的小鼠直系同源物,Lsm4p是一种在酵母和人类细胞中发现的蛋白质,可能与U6 snRNA相关。在小鼠Lsm4(mLsm4)内源性启动子控制下引入geo报告基因盒表明该基因在胚胎和成年组织中普遍转录。geo盒的插入破坏了mLsm4等位基因,该突变的纯合性导致隐性胚胎致死表型。mLsm4基因敲除的合子存活到囊胚阶段,植入子宫,但此后不久死亡。mLsm4p基因敲除小鼠的早期死亡表明mLsm4p在剪接中的作用至关重要,不能被其他Lsm蛋白补偿。

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