Interaction between the Drosophila CAF-1 and ASF1 Chromatin Assembly Factors

Author:

Tyler Jessica K.12,Collins Kimberly A.1,Prasad-Sinha Jayashree3,Amiott Elizabeth2,Bulger Michael1,Harte Peter J.3,Kobayashi Ryuji4,Kadonaga James T.1

Affiliation:

1. Section of Molecular Biology, University of California, San Diego, La Jolla, California 92093-0347 1 ;

2. Department of Biochemistry and Molecular Genetics, University of Colorado Health Sciences Center, Denver, Colorado 80262 2 ;

3. Department of Genetics, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106 3 ; and

4. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York 117244

Abstract

ABSTRACT The assembly of newly synthesized DNA into chromatin is essential for normal growth, development, and differentiation. To gain a better understanding of the assembly of chromatin during DNA synthesis, we identified, cloned, and characterized the 180- and 105-kDa polypeptides of Drosophila chromatin assembly factor 1 (dCAF-1). The purified recombinant p180+p105+p55 dCAF-1 complex is active for DNA replication-coupled chromatin assembly. Furthermore, we have established that the putative 75-kDa polypeptide of dCAF-1 is a C-terminally truncated form of p105 that does not coexist in dCAF-1 complexes containing the p105 subunit. The analysis of native and recombinant dCAF-1 revealed an interaction between dCAF-1 and the Drosophila anti-silencing function 1 (dASF1) component of replication-coupling assembly factor (RCAF). The binding of dASF1 to dCAF-1 is mediated through the p105 subunit of dCAF-1. Consistent with the interaction between dCAF-1 p105 and dASF1 in vitro, we observed that dASF1 and dCAF-1 p105 colocalized in vivo in Drosophila polytene chromosomes. This interaction between dCAF-1 and dASF1 may be a key component of the functional synergy observed between RCAF and dCAF-1 during the assembly of newly synthesized DNA into chromatin.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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