Schubert S, Skawran B, Dechend F, Nayernia K, Meinhardt A, Nanda I, Schmid M, Engel W, Schmidtke J
Institute of Human Genetics, Hannover Medical School, D-30623 Hannover, Germany.
Biol Reprod. 2003 Sep;69(3):968-75. doi: 10.1095/biolreprod.103.016501. Epub 2003 May 28.
To generate an animal model that is suitable for the analysis of regulation and expression of human testis-specific protein, Y-encoded TSPY, a transgenic mouse line, TgTSPY9, harboring a complete structural human TSPY gene was generated. Fluorescence in situ hybridization and Southern analyses show that approximately 50 copies of the human TSPY transgene are integrated at a single chromosomal site that maps to the distal long arm of the Y chromosome. The transgene is correctly transcribed and spliced according to the human pattern and is mainly expressed in testicular tissue, with spermatogonia and early primary spermatocytes (leptotene and zygotene) as expressing germ cells. TSPY transgenic mice are phenotypically normal, and spermatogenesis is neither impaired nor enhanced by the human transgene. The present study shows that a human TSPY gene integrated into the mouse genome follows the human expression pattern although murine tspy had lost its function in rodent evolution millions of years ago.
为了生成一个适合分析人类睾丸特异性蛋白(Y编码的TSPY)调控和表达的动物模型,我们构建了一个携带完整人类TSPY基因结构的转基因小鼠品系TgTSPY9。荧光原位杂交和Southern分析表明,约50个拷贝的人类TSPY转基因整合在一个单一的染色体位点上,该位点定位于Y染色体长臂远端。转基因按照人类模式正确转录和剪接,主要在睾丸组织中表达,精原细胞和早期初级精母细胞(细线期和偶线期)为表达的生殖细胞。TSPY转基因小鼠在表型上是正常的,人类转基因既不损害也不增强精子发生。本研究表明,尽管小鼠tspy在数百万年前的啮齿动物进化中失去了功能,但整合到小鼠基因组中的人类TSPY基因遵循人类表达模式。