Jankowski C, Nasar F, Nag D K
Molecular Genetics Program, Wadsworth Center, 120 New Scotland Avenue, Albany, NY 12201-2002, USA.
Proc Natl Acad Sci U S A. 2000 Feb 29;97(5):2134-9. doi: 10.1073/pnas.040460297.
Expansion of trinucleotide repeats is associated with a growing number of human diseases. The mechanism and timing of expansion of the repeat tract are poorly understood. In humans, trinucleotide repeats show extreme meiotic instability, and expansion of the repeat tract has been suggested to occur in the germ-line mitotic divisions or postmeiotically during early divisions of the embryo. Studies in model organisms have indicated that polymerase slippage plays a major role in the repeat tract instability and meiotic instability is severalfold higher than the mitotic instability. We show here that meiotic instability of the CAG/CTG repeat tract in yeast is associated with double-strand break (DSB) formation within the repeated sequences, and that the DSB formation is dependent on the meiotic recombination machinery. The DSB repair results in both expansions and contractions of the CAG repeat tract.
三核苷酸重复序列的扩增与越来越多的人类疾病相关。重复序列扩增的机制和时间尚不清楚。在人类中,三核苷酸重复序列表现出极端的减数分裂不稳定性,重复序列的扩增被认为发生在生殖系有丝分裂或胚胎早期分裂的减数分裂后。对模式生物的研究表明,聚合酶滑动在重复序列不稳定性中起主要作用,减数分裂不稳定性比有丝分裂不稳定性高几倍。我们在此表明,酵母中CAG/CTG重复序列的减数分裂不稳定性与重复序列内双链断裂(DSB)的形成有关,并且DSB的形成依赖于减数分裂重组机制。DSB修复导致CAG重复序列的扩增和收缩。