Species comparison of protein synthesis accuracy.

Advances in pathobiology Pub Date : 1980-01-01
G P Hirsch, R A Popp, M C Francis, B S Bradshaw, E G Bailiff
{"title":"Species comparison of protein synthesis accuracy.","authors":"G P Hirsch,&nbsp;R A Popp,&nbsp;M C Francis,&nbsp;B S Bradshaw,&nbsp;E G Bailiff","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The average accuracy of protein synthesis in reticulocytes from several mammalian species does not correlate with longevity potential from 13 to 90 years. Isoleucine incorporation into highly purified hemoglobin chains which contain no genetically coded isoleucine was used as a direct test of protein synthesis accuracy. Since isoleucine can be incorporated into these molecules by mutations in a few cells as well as errors in most cells, the constant level of isoleucine substitution may also show that the mutation rates are not dramatically different among these species. Isoleucine substitutions in hemoglobin can be used to estimate mutations only above the level of errors, which may be as low as 1/1,000,000, but the probability of seeing a few mutant clones at any time is dependent on the number of stem cells producing reticulocytes. The number of stem cells being expressed is a reflection of the number of cell divisions per clone. If the number of cell divisions per clone is 30 or less, then isoleucine substitutions would increase when the mutation accumulation rose above 30 per million for the mutation to isoleucine at any position in the alpha or beta chain.</p>","PeriodicalId":75448,"journal":{"name":"Advances in pathobiology","volume":"7 ","pages":"142-59"},"PeriodicalIF":0.0000,"publicationDate":"1980-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in pathobiology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The average accuracy of protein synthesis in reticulocytes from several mammalian species does not correlate with longevity potential from 13 to 90 years. Isoleucine incorporation into highly purified hemoglobin chains which contain no genetically coded isoleucine was used as a direct test of protein synthesis accuracy. Since isoleucine can be incorporated into these molecules by mutations in a few cells as well as errors in most cells, the constant level of isoleucine substitution may also show that the mutation rates are not dramatically different among these species. Isoleucine substitutions in hemoglobin can be used to estimate mutations only above the level of errors, which may be as low as 1/1,000,000, but the probability of seeing a few mutant clones at any time is dependent on the number of stem cells producing reticulocytes. The number of stem cells being expressed is a reflection of the number of cell divisions per clone. If the number of cell divisions per clone is 30 or less, then isoleucine substitutions would increase when the mutation accumulation rose above 30 per million for the mutation to isoleucine at any position in the alpha or beta chain.

物种蛋白质合成精度的比较。
几种哺乳动物网织红细胞中蛋白质合成的平均准确度与13至90岁的潜在寿命无关。异亮氨酸掺入不含遗传编码异亮氨酸的高纯度血红蛋白链中,作为蛋白质合成准确性的直接测试。由于异亮氨酸可以通过少数细胞的突变和大多数细胞的错误被纳入这些分子中,因此恒定水平的异亮氨酸替代也可能表明这些物种之间的突变率没有显着差异。血红蛋白中的异亮氨酸替代可以用来估计突变,仅高于误差水平,其可能低至1/1,000,000,但是在任何时候看到一些突变克隆的概率取决于产生网状红细胞的干细胞的数量。被表达的干细胞数量反映了每个克隆细胞分裂的数量。如果每个克隆的细胞分裂数为30或更少,那么当突变积累超过30 /百万时,在α链或β链的任何位置突变为异亮氨酸时,异亮氨酸替代将增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信