Seabury Christopher M, Honeycutt Rodney L, Rooney Alejandro P, Halbert Natalie D, Derr James N
Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843-4467, USA.
Proc Natl Acad Sci U S A. 2004 Oct 19;101(42):15142-7. doi: 10.1073/pnas.0406403101. Epub 2004 Oct 11.
Amino acid replacements encoded by the prion protein gene (PRNP) have been associated with transmissible and hereditary spongiform encephalopathies in mammalian species. However, an association between bovine spongiform encephalopathy (BSE) and bovine PRNP exon 3 has not been detected. Moreover, little is currently known regarding the mechanisms of evolution influencing the bovine PRNP gene. Therefore, in this study we evaluated the patterns of nucleotide variation associated with PRNP exon 3 for 36 breeds of domestic cattle and representative samples for 10 additional species of Bovinae. The results of our study indicate that strong purifying selection has intensely constrained PRNP over the long-term evolutionary history of the subfamily Bovinae, especially in regions considered to be of functional, structural, and pathogenic importance in humans as well as other mammals. The driving force behind this intense level of purifying selection remains to be explained.
朊病毒蛋白基因(PRNP)编码的氨基酸替换与哺乳动物的传染性和遗传性海绵状脑病有关。然而,尚未检测到牛海绵状脑病(BSE)与牛PRNP外显子3之间的关联。此外,目前对于影响牛PRNP基因的进化机制知之甚少。因此,在本研究中,我们评估了36个家牛品种以及另外10种牛亚科代表性样本中与PRNP外显子3相关的核苷酸变异模式。我们的研究结果表明,在牛亚科的长期进化历史中,强烈的纯化选择对PRNP进行了严格的限制,特别是在被认为对人类以及其他哺乳动物具有功能、结构和致病重要性的区域。这种强烈纯化选择水平背后的驱动力仍有待解释。