Multivalent interaction of ESCO2 with the replication machinery is required for sister chromatid cohesion in vertebrates

被引:32
作者
Bender, Dawn [1 ,2 ]
Da Silva, Eulalia Maria Lima [1 ]
Chen, Jingrong [1 ]
Poss, Annelise [1 ]
Gawey, Lauren [1 ]
Rulon, Zane [1 ]
Rankin, Susannah [1 ,2 ]
机构
[1] Oklahoma Med Res Fdn, Program Cell Cycle & Canc Biol, Oklahoma City, OK 73104 USA
[2] Oklahoma Univ, Hlth Sci Ctr, Dept Cell Biol, Oklahoma City, OK 73104 USA
关键词
chromosome biology; DNA replication; cohesin; sister chromatid cohesion; DNA-DAMAGE RESPONSE; DISORDERED PROTEIN; PIP-BOX; S-PHASE; PCNA; ESTABLISHMENT; ACETYLATION; BINDING; SITES; ACTIVATION;
D O I
10.1073/pnas.1911936117
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The tethering together of sister chromatids by the cohesin complex ensures their accurate alignment and segregation during cell division. In vertebrates, sister chromatid cohesion requires the activity of the ESCO2 acetyltransferase, which modifies the Smc3 subunit of cohesin. It was shown recently that ESCO2 promotes cohesion through interaction with the MCM replicative helicase. However, ESCO2 does not significantly colocalize with the MCM complex, suggesting there are additional interactions important for ESCO2 function. Here we show that ESCO2 is recruited to replication factories, sites of DNA replication, through interaction with PCNA. We show that ESCO2 contains multiple PCNA-interaction motifs in its N terminus, each of which is essential to its ability to establish cohesion. We propose that multiple PCNA-interaction motifs embedded in a largely flexible and disordered region of the protein underlie the unique ability of ESCO2 to establish cohesion between sister chromatids precisely as they are born during DNA replication.
引用
收藏
页码:1081 / 1089
页数:9
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