Kimura Motoshi I, Kazuki Yasuhiro, Kashiwagi Akiko, Kai Yoshiteru, Abe Satoshi, Barbieri Ottavia, Levi Giovanni, Oshimura Mitsuo
Institute of Regenerative Medicine and Biofunction, Graduate School of Medical Science, Tottori University, 86 Nishimachi, Yonago 683-8503, Japan.
J Hum Genet. 2004;49(5):273-7. doi: 10.1007/s10038-004-0139-2.
The mouse Dlx5 gene encodes a distal-less-related DNA-binding homeobox protein first expressed during early embryonic development in anterior regions of mouse embryo and is located on chromosome 6, which is the syntenic region to the human chromosome 7q21-q31 imprinting cluster. Recently, its human homologue, DLX5, was identified to be imprinted and maternally expressed, at least in normal human lymphoblasts and in brain tissues. In our study, we analyzed the imprinting status of mouse Dlx5 by RT-PCR, first in the F1 of a reciprocal cross between two different mouse strains, and second in heterozygous Dlx5 mutant mice. Both approaches revealed that mouse Dlx5 followed a biallelic pattern of expression in brain tissue and in testis. Our findings suggest that the Dlx5 gene escapes genomic imprinting, at least in mice of certain genetic backgrounds.
小鼠Dlx5基因编码一种与远端缺失相关的DNA结合同源框蛋白,该蛋白最早在小鼠胚胎前部的早期胚胎发育过程中表达,位于6号染色体上,该区域与人类染色体7q21-q31印记簇是同线性区域。最近,其人类同源物DLX5被鉴定为印记基因且由母系表达,至少在正常人淋巴细胞和脑组织中如此。在我们的研究中,我们首先通过RT-PCR分析了两种不同小鼠品系正反交F1代中,其次在杂合Dlx5突变小鼠中,小鼠Dlx5的印记状态。两种方法均显示,小鼠Dlx5在脑组织和睾丸中遵循双等位基因表达模式。我们的研究结果表明,Dlx5基因至少在某些遗传背景的小鼠中逃避了基因组印记。