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再探超氧化物歧化酶分子时钟

The superoxide dismutase molecular clock revisited.

作者信息

Fitch W M, Ayala F J

机构信息

Department of Ecology and Evolutionary Biology, University of California, Irvine 92717.

出版信息

Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):6802-7. doi: 10.1073/pnas.91.15.6802.

Abstract

The Cu,Zn superoxide dismutase (SOD) was examined earlier and found to behave in a very unclock-like manner despite (accepted point mutation, or PAM) corrections for multiple replacements per site. Depending upon the time span involved, rates could differ 5-fold. We have sought to determine whether the data might be clock-like if a covarion model were used. We first determined that the number of concomitantly variable codons (covarions) in SOD is 28. With that value fixed we found that the observations for SOD could fit reasonably well a molecular clock if, given 28 covarions, (i) there are approximately six replacements every 10 million years, (ii) the total number of codons is 162, (iii) the number of codons that are permanently invariable across the range of taxa from fungi to mammals is 44, and (iv) the persistence of variability is quite low (0.01). Thus, the inconsistent number of amino acid differences between various pairs of descendent sequences could well be the result of a fairly accurate molecular clock. The general conclusion has two sides: (i) the inference that a given gene is a bad clock may sometimes arise through a failure to take all the relevant biology into account and (ii) one should examine the possibility that different subsets of amino acids are evolving at different rates, because otherwise the assumption of a clock may yield erroneous estimates of divergence times on the basis of the observed number of amino acid differences.

摘要

早期对铜锌超氧化物歧化酶(SOD)进行了研究,发现尽管对每个位点的多个替换进行了(公认的点突变或PAM)校正,但其行为方式却非常不像时钟。根据所涉及的时间跨度,速率可能相差5倍。我们试图确定,如果使用共变模型,数据是否可能类似时钟。我们首先确定SOD中共变密码子(共变位点)的数量为28个。固定该值后,我们发现,如果给定28个共变位点,SOD的观测结果可以相当好地拟合分子时钟,条件如下:(i)每1000万年大约有6个替换;(ii)密码子总数为162个;(iii)从真菌到哺乳动物的分类群范围内永久不变的密码子数量为44个;(iv)变异性的持续性相当低(0.01)。因此,不同后代序列对之间氨基酸差异数量的不一致很可能是相当准确的分子时钟的结果。总体结论有两个方面:(i)认为某个特定基因不是一个好时钟的推断有时可能是由于没有考虑到所有相关生物学因素;(ii)应该研究氨基酸的不同子集以不同速率进化的可能性,因为否则基于观察到的氨基酸差异数量的时钟假设可能会产生错误的分歧时间估计。

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The superoxide dismutase molecular clock revisited.再探超氧化物歧化酶分子时钟
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本文引用的文献

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On the virtues and pitfalls of the molecular evolutionary clock.论分子进化钟的优点与缺陷
J Hered. 1986 Jul-Aug;77(4):226-35. doi: 10.1093/oxfordjournals.jhered.a110227.

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