Reynolds John J, El-Khamisy Sherif F, Katyal Sachin, Clements Paula, McKinnon Peter J, Caldecott Keith W
Genome Damage and Stability Centre, University of Sussex, Science Park Road, Falmer, Brighton BN1 9RQ, United Kingdom.
Mol Cell Biol. 2009 Mar;29(5):1354-62. doi: 10.1128/MCB.01471-08. Epub 2008 Dec 22.
Ataxia oculomotor apraxia 1 (AOA1) results from mutations in aprataxin, a component of DNA strand break repair that removes AMP from 5' termini. Despite this, global rates of chromosomal strand break repair are normal in a variety of AOA1 and other aprataxin-defective cells. Here we show that short-patch single-strand break repair (SSBR) in AOA1 cell extracts bypasses the point of aprataxin action at oxidative breaks and stalls at the final step of DNA ligation, resulting in the accumulation of adenylated DNA nicks. Strikingly, this defect results from insufficient levels of nonadenylated DNA ligase, and short-patch SSBR can be restored in AOA1 extracts, independently of aprataxin, by the addition of recombinant DNA ligase. Since adenylated nicks are substrates for long-patch SSBR, we reasoned that this pathway might in part explain the apparent absence of a chromosomal SSBR defect in aprataxin-defective cells. Indeed, whereas chemical inhibition of long-patch repair did not affect SSBR rates in wild-type mouse neural astrocytes, it uncovered a significant defect in Aptx(-/-) neural astrocytes. These data demonstrate that aprataxin participates in chromosomal SSBR in vivo and suggest that short-patch SSBR arrests in AOA1 because of insufficient nonadenylated DNA ligase.
眼动失用性共济失调1型(AOA1)是由脱嘌呤嘧啶核酸内切酶(aprataxin)突变引起的,aprataxin是DNA链断裂修复的一个组成部分,可从5'末端去除AMP。尽管如此,在多种AOA1细胞和其他脱嘌呤嘧啶核酸内切酶缺陷细胞中,染色体链断裂修复的整体速率是正常的。在这里,我们表明,AOA1细胞提取物中的短片段单链断裂修复(SSBR)绕过了脱嘌呤嘧啶核酸内切酶在氧化断裂处的作用点,并在DNA连接的最后一步停滞,导致腺苷酸化DNA切口的积累。令人惊讶的是,这种缺陷是由于未腺苷酸化的DNA连接酶水平不足导致的,并且通过添加重组DNA连接酶,短片段SSBR可以在AOA1提取物中独立于脱嘌呤嘧啶核酸内切酶而恢复。由于腺苷酸化切口是长片段SSBR的底物,我们推测这条途径可能部分解释了脱嘌呤嘧啶核酸内切酶缺陷细胞中染色体SSBR缺陷明显缺失的原因。事实上,虽然化学抑制长片段修复并不影响野生型小鼠神经星形胶质细胞中的SSBR速率,但它揭示了Aptx(-/-)神经星形胶质细胞中存在明显缺陷。这些数据表明,脱嘌呤嘧啶核酸内切酶在体内参与染色体SSBR,并表明短片段SSBR在AOA1中停滞是由于未腺苷酸化的DNA连接酶不足。