CENP-A arrays are more condensed than canonical arrays at low ionic strength.

Abstract:

:The centromeric histone H3 variant centromeric protein A (CENP-A), whose sequence is the least conserved among all histone variants, is responsible for specifying the location of the centromere. Here, we present a comprehensive study of CENP-A nucleosome arrays by cryo-electron tomography. We see that CENP-A arrays have different biophysical properties than canonical ones under low ionic conditions, as they are more condensed with a 20% smaller average nearest-neighbor distance and a 30% higher nucleosome density. We find that CENP-A nucleosomes have a predominantly crossed DNA entry/exit site that is narrowed on average by 8°, and they have a propensity to stack face to face. We therefore propose that CENP-A induces geometric constraints at the nucleosome DNA entry/exit site to bring neighboring nucleosomes into close proximity. This specific property of CENP-A may be responsible for generating a fundamental process that contributes to increased chromatin fiber compaction that is propagated under physiological conditions to form centromeric chromatin.

journal_name

Biophys J

journal_title

Biophysical journal

authors

Geiss CP,Keramisanou D,Sekulic N,Scheffer MP,Black BE,Frangakis AS

doi

10.1016/j.bpj.2014.01.005

subject

Has Abstract

pub_date

2014-02-18 00:00:00

pages

875-82

issue

4

eissn

0006-3495

issn

1542-0086

pii

S0006-3495(14)00063-0

journal_volume

106

pub_type

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