Zou S, Voytas D F
Department of Zoology and Genetics, Iowa State University, Ames, IA 50011, USA.
Proc Natl Acad Sci U S A. 1997 Jul 8;94(14):7412-6. doi: 10.1073/pnas.94.14.7412.
The HML and HMR mating loci of Saccharomyces cerevisiae are bound in silent chromatin, which is assembled at the flanking E and I transcriptional silencers. The retrotransposon Ty5 preferentially integrates into regions of silent chromatin, and Ty5 insertions near the HMR-E silencer account for approximately 2% of total transposition events. Most Ty5 insertions occur within 800 bp on either side of the autonomously replicating consensus sequence within HMR-E. Ty5 target preference is determined by silent chromatin, because integration near HMR-E is abolished in strains with silencer mutations that alleviate transcriptional repression. The recognition of specific DNA sequences per se does not direct integration, rather, it is the protein complex assembled at the silencers. As demonstrated here for Ty5, recognition of specific chromatin domains may be a general mechanism by which retrotransposons and retroviruses determine integration sites.
酿酒酵母的HML和HMR交配位点被沉默染色质所结合,沉默染色质在侧翼的E和I转录沉默子处组装。逆转座子Ty5优先整合到沉默染色质区域,HMR-E沉默子附近的Ty5插入约占总转座事件的2%。大多数Ty5插入发生在HMR-E内自主复制共有序列两侧800 bp范围内。Ty5的靶标偏好由沉默染色质决定,因为在具有减轻转录抑制的沉默子突变的菌株中,HMR-E附近的整合被消除。对特定DNA序列本身的识别并不指导整合,相反,是在沉默子处组装的蛋白质复合物起作用。如本文对Ty5的证明,对特定染色质结构域的识别可能是逆转座子和逆转录病毒确定整合位点的普遍机制。