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Molecular and Cellular Biology, June 1999, p. 4366-4378, Vol. 19, No. 6
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
KAP-1 Corepressor Protein Interacts and Colocalizes with
Heterochromatic and Euchromatic HP1 Proteins: a Potential Role for
Krüppel-Associated Box-Zinc Finger Proteins in
Heterochromatin-Mediated Gene Silencing
Robert F.
Ryan,1
David C.
Schultz,1
Kasirajan
Ayyanathan,1
Prim B.
Singh,2
Josh R.
Friedman,1
William J.
Fredericks,3 and
Frank J.
Rauscher III1,*
The Wistar Institute, Philadelphia,
Pennsylvania1; Department of Development
and Reproduction, The Roslin Institute, Edinburgh, United
Kingdom2; and Onyx Pharmaceuticals,
Richmond, California3
Received 28 December 1998/Returned for modification 8 February
1999/Accepted 29 February 1999
Krüppel-associated box (KRAB) domains are present in
approximately one-third of all human zinc finger proteins (ZFPs) and are potent transcriptional repression modules. We have previously cloned a corepressor for the KRAB domain, KAP-1, which is required for
KRAB-mediated repression in vivo. To characterize the repression mechanism utilized by KAP-1, we have analyzed the ability of KAP-1 to
interact with murine (M31 and M32) and human (HP1
and HP1
) homologues of the HP1 protein family, a class of nonhistone
heterochromatin-associated proteins with a well-established epigenetic
gene silencing function in Drosophila. In vitro studies
confirmed that KAP-1 is capable of directly interacting with M31 and
hHP1
, which are normally found in centromeric heterochromatin, as
well as M32 and hHP1
, both of which are found in euchromatin.
Mapping of the region in KAP-1 required for HP1 interaction showed that
amino acid substitutions which abolish HP1 binding in vitro reduce
KAP-1 mediated repression in vivo. We observed colocalization of KAP-1
with M31 and M32 in interphase nuclei, lending support to the
biochemical evidence that M31 and M32 directly interact with KAP-1. The
colocalization of KAP-1 with M31 is sometimes found in subnuclear
territories of potential pericentromeric heterochromatin, whereas
colocalization of KAP-1 and M32 occurs in punctate euchromatic domains
throughout the nucleus. This work suggests a mechanism for the
recruitment of HP1-like gene products by the KRAB-ZFP-KAP-1 complex to
specific loci within the genome through formation of
heterochromatin-like complexes that silence gene activity. We speculate
that gene-specific repression may be a consequence of the formation of
such complexes, ultimately leading to silenced genes in newly formed
heterochromatic chromosomal environments.
*
Corresponding author. Mailing address: The Wistar
Institute, 3601 Spruce St., Philadelphia, PA 19104. Phone: (215)
898-0995. Fax: (215) 898-3929. E-mail:
Rauscher{at}wista.wistar.upenn.edu.
Molecular and Cellular Biology, June 1999, p. 4366-4378, Vol. 19, No. 6
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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