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Identification of Noncoding Transcripts from within CENP-A Chromatin at Fission Yeast Centromeres
被引:97
作者:
Choi, Eun Shik
[2
,3
]
Stralfors, Annelie
[1
]
Castillo, Araceli G.
[2
,3
]
Durand-Dubief, Mickael
[1
]
Ekwall, Karl
[1
]
Allshire, Robin C.
[2
,3
]
机构:
[1] Karolinska Inst, Novum, Dept Biosci & Nutr, Ctr Biosci, S-14157 Huddinge, Sweden
[2] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[3] Univ Edinburgh, Inst Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
基金:
英国惠康基金;
瑞典研究理事会;
关键词:
COMPREHENSIVE ANALYSIS;
EPIGENETIC REGULATION;
RNA;
HETEROCHROMATIN;
PROTEIN;
GENE;
KINETOCHORES;
COMPONENTS;
TURNOVER;
DYNAMICS;
D O I:
10.1074/jbc.M111.228510
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The histone H3 variant CENP-A is the most favored candidate for an epigenetic mark that specifies the centromere. In fission yeast, adjacent heterochromatin can direct CENP-A(Cnp1) chromatin establishment, but the underlying features governing where CENP-A(Cnp1) chromatin assembles are unknown. We show that, in addition to centromeric regions, a low level of CENP-A(Cnp1) associates with gene promoters where histone H3 is depleted by the activity of the Hrp1(Chd1) chromatin-remodeling factor. Moreover, we demonstrate that noncoding RNAs are transcribed by RNA polymerase II (RNAPII) from CENP-A(Cnp1) chromatin at centromeres. These analyses reveal a similarity between centromeres and a subset of RNAPII genes and suggest a role for remodeling at RNAPII promoters within centromeres that influences the replacement of histone H3 with CENP-A(Cnp1).
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页码:23600 / 23607
页数:8
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