Author:
Kim Jung-Hyun,Ebersole Thomas,Kouprina Natalay,Noskov Vladimir N.,Ohzeki Jun-Ichirou,Masumoto Hiroshi,Mravinac Brankica,Sullivan Beth A.,Pavlicek Adam,Dovat Sinisa,Pack Svetlana D.,Kwon Yoo-Wook,Flanagan Patrick T.,Loukinov Dmitri,Lobanenkov Victor,Larionov Vladimir
Abstract
The role of repetitive DNA sequences in pericentromeric regions with respect to kinetochore/heterochromatin structure and function is poorly understood. Here, we use a mouse erythroleukemia cell (MEL) system for studying how repetitive DNA assumes or is assembled into different chromatin structures. We show that human gamma-satellite DNA arrays allow a transcriptionally permissive chromatin conformation in an adjacent transgene and efficiently protect it from epigenetic silencing. These arrays contain CTCF and Ikaros binding sites. In MEL cells, this gamma-satellite DNA activity depends on binding of Ikaros proteins involved in differentiation along the hematopoietic pathway. Given our discovery of gamma-satellite DNA in pericentromeric regions of most human chromosomes and a dynamic chromatin state of gamma-satellite arrays in their natural location, we suggest that gamma-satellite DNA represents a unique region of the functional centromere with a possible role in preventing heterochromatin spreading beyond the pericentromeric region.
Publisher
Cold Spring Harbor Laboratory
Subject
Genetics (clinical),Genetics
Cited by
56 articles.
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