Roshon Michael J, Ruley H Earl
Department of Microbiology and Immunology, Room AA4210 MCN, Vanderbilt University School of Medicine, 1161 21st Ave South, Nashville, TN 37232-2363, USA.
Transgenic Res. 2005 Apr;14(2):179-92. doi: 10.1007/s11248-004-8147-8.
The present study characterized an embryonic lethal mutation induced by insertion of the U3Neo gene trap retrovirus into an intron of the gene encoding heterogeneous ribonuclear protein U (Hnrnpu), which maps to the distal arm of mouse chromosome 1. Murine hnRNP U was found to be identical to the human protein at all but one of 341 amino acid residues. Embryos homozygous for the provirus showed obvious abnormalities after 6.5 days of development (E6.5) and were resorbed by E10.5. Expression of the inserted neomycin-resistance gene involved alternative splicing to a cryptic 3' splice site located in the neomycin resistance gene resulting in a hypomorphic mutation. Homozygous mutant cell lines isolated from preimplantation blastocysts expressed hnRNP U transcripts at levels 2 to 5 times lower than wild-type cells, suggesting that nearly wild-type levels of hnRNP U are required for embryonic development.
本研究对一种胚胎致死突变进行了特征描述,该突变是由U3Neo基因捕获逆转录病毒插入编码异质性核糖核蛋白U(Hnrnpu)的基因内含子所致,该基因定位于小鼠1号染色体的远端臂。发现鼠源hnRNP U与人类蛋白在341个氨基酸残基中除一个以外的所有残基上均相同。携带前病毒的纯合胚胎在发育6.5天(E6.5)后出现明显异常,并在E10.5时被吸收。插入的新霉素抗性基因的表达涉及到与新霉素抗性基因中一个隐蔽的3'剪接位点的可变剪接,从而导致一个亚效突变。从植入前囊胚中分离出的纯合突变细胞系表达hnRNP U转录本的水平比野生型细胞低2至5倍,这表明胚胎发育需要近乎野生型水平的hnRNP U。