Shitara H, Hayashi J I, Takahama S, Kaneda H, Yonekawa H
Institute of Biological Sciences, University of Tsukuba, Ibaraki, Japan.
Genetics. 1998 Feb;148(2):851-7. doi: 10.1093/genetics/148.2.851.
The transmission profiles of sperm mtDNA introduced into fertilized eggs were examined in detail in F1 hybrids of mouse interspecific crosses by addressing three aspects. The first is whether the leaked paternal mtDNA in fertilized eggs produced by interspecific crosses was distributed stably to all tissues after the eggs' development to adults. The second is whether the leaked paternal mtDNA was transmitted to the subsequent generations. The third is whether paternal mtDNA continuously leaks in subsequent backcrosses. For identification of the leaked paternal mtDNA, we prepared total DNA samples directly from tissues or embryos and used PCR techniques that can detect a few molecules of paternal mtDNA even in the presence of 10(8)-fold excess of maternal mtDNA. The results showed that the leaked paternal mtDNA was not distributed to all tissues in the F1 hybrids or transmitted to the following generations through the female germ line. Moreover, the paternal mtDNA leakage was limited to the first generation of an interspecific cross and did not occur in progeny from subsequent backcrosses. These observations suggest that species-specific exclusion of sperm mtDNA in mammalian fertilized eggs is extremely stringent, ensuring strictly maternal inheritance of mtDNA.
通过研究三个方面,详细检测了导入受精卵的精子线粒体DNA(mtDNA)在小鼠种间杂交F1代杂种中的传递情况。第一,种间杂交产生的受精卵中泄漏的父本mtDNA在卵子发育为成体后是否稳定地分布于所有组织。第二,泄漏的父本mtDNA是否传递给后代。第三,父本mtDNA在后续回交中是否持续泄漏。为了鉴定泄漏的父本mtDNA,我们直接从组织或胚胎中制备总DNA样本,并使用PCR技术,即使在母本mtDNA过量10^8倍的情况下,该技术也能检测到少量父本mtDNA分子。结果表明,泄漏的父本mtDNA在F1代杂种中并非分布于所有组织,也未通过雌性生殖系传递给后代。此外,父本mtDNA泄漏仅限于种间杂交的第一代,在后续回交后代中并未发生。这些观察结果表明,哺乳动物受精卵中精子mtDNA的种属特异性排除极为严格,并确保了mtDNA严格的母系遗传。