Singh Amit Kumar, Bashir Tufail, Sailer Christian, Gurumoorthy Viswanathan, Ramakrishnan Anantha Maharasi, Dhanapal Shanmuhapreya, Grossniklaus Ueli, Baskar Ramamurthy
Department of Biotechnology, Indian Institute of Technology-Madras, Chennai 600 036, India (A.K.S., T.B., V.G., A.M.R., S.D., R.B.); andInstitute of Plant Biology and Zurich-Basel Plant Science Center, University of Zurich, CH-8008 Zurich, Switzerland (C.S., U.G.).
Department of Biotechnology, Indian Institute of Technology-Madras, Chennai 600 036, India (A.K.S., T.B., V.G., A.M.R., S.D., R.B.); andInstitute of Plant Biology and Zurich-Basel Plant Science Center, University of Zurich, CH-8008 Zurich, Switzerland (C.S., U.G.)
Plant Physiol. 2015 May;168(1):247-57. doi: 10.1104/pp.15.00291. Epub 2015 Mar 25.
In humans, it is well known that the parental reproductive age has a strong influence on mutations transmitted to their progeny. Meiotic nondisjunction is known to increase in older mothers, and base substitutions tend to go up with paternal reproductive age. Hence, it is clear that the germinal mutation rates are a function of both maternal and paternal ages in humans. In contrast, it is unknown whether the parental reproductive age has an effect on somatic mutation rates in the progeny, because these are rare and difficult to detect. To address this question, we took advantage of the plant model system Arabidopsis (Arabidopsis thaliana), where mutation detector lines allow for an easy quantitation of somatic mutations, to test the effect of parental age on somatic mutation rates in the progeny. Although we found no significant effect of parental age on base substitutions, we found that frameshift mutations and transposition events increased in the progeny of older parents, an effect that is stronger through the maternal line. In contrast, intrachromosomal recombination events in the progeny decrease with the age of the parents in a parent-of-origin-dependent manner. Our results clearly show that parental reproductive age affects somatic mutation rates in the progeny and, thus, that some form of age-dependent information, which affects the frequency of double-strand breaks and possibly other processes involved in maintaining genome integrity, is transmitted through the gametes.
在人类中,众所周知,父母的生殖年龄对传递给后代的突变有很大影响。已知减数分裂不分离在年龄较大的母亲中会增加,而碱基替换往往会随着父亲生殖年龄的增加而上升。因此,很明显,人类的生殖细胞突变率是母亲和父亲年龄的函数。相比之下,尚不清楚父母的生殖年龄是否会对后代的体细胞突变率产生影响,因为这些突变很少见且难以检测。为了解决这个问题,我们利用植物模式系统拟南芥(Arabidopsis thaliana),其中突变检测系允许轻松定量体细胞突变,以测试亲本年龄对后代体细胞突变率的影响。虽然我们没有发现亲本年龄对碱基替换有显著影响,但我们发现移码突变和转座事件在年龄较大的亲本的后代中增加,这种影响通过母系更强。相比之下,后代中的染色体内重组事件以亲本来源依赖的方式随着亲本年龄的增加而减少。我们的结果清楚地表明,父母的生殖年龄会影响后代的体细胞突变率,因此,某种形式的年龄依赖性信息,它影响双链断裂的频率以及可能参与维持基因组完整性的其他过程,通过配子传递。