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Genome Res. 13:1416-1429, 2003 ©2003 by Cold Spring Harbor Laboratory Press; ISSN 1088-9051/03 $5.00 Letter Identification and Analysis of Chromodomain-Containing Proteins Encoded in the Mouse Transcriptome1ARC Special Research Centre for Functional and Applied Genomics, Institute for Molecular Bioscience, University of Queensland, St.Lucia, Queensland 4072, Australia 2School of Molecular and Microbial Sciences, University of Queensland, St.Lucia, Queensland 4072, Australia 3Laboratory for Genome Exploration Research Group, RIKEN Genomic Sciences Center (GSC), RIKEN Yokohama Institute, Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, 230-0045, Japan 4Genome Science Laboratory, RIKEN, Hirosawa, Wako, Saitama 351-0198, Japan
The chromodomain is 4050 amino acids in length and is conserved in a wide range of chromatic and regulatory proteins involved in chromatin remodeling. Chromodomain-containing proteins can be classified into families based on their broader characteristics, in particular the presence of other types of domains, and which correlate with different subclasses of the chromodomains themselves. Hidden Markov model (HMM)-generated profiles of different subclasses of chromodomains were used here to identify sequences encoding chromodomain-containing proteins in the mouse transcriptome and genome. A total of 36 different loci encoding proteins containing chromodomains, including 17 novel loci, were identified. Six of these loci (including three apparent pseudogenes, a novel HP1 ortholog, and two novel Msl-3 transcription factor-like proteins) are not present in the human genome, whereas the human genome contains four loci (two CDY orthologs and two apparent CDY pseudogenes) that are not present in mouse. A number of these loci exhibit alternative splicing to produce different isoforms, including 43 novel variants, some of which lack the chromodomain. The likely functions of these proteins are discussed in relation to the known functions of other chromodomain-containing proteins within the same family.
Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.1015703. 5 Takahiro Arakawa, Piero Carninci, Jun Kawai, and Yoshihide Hayashizaki.
6 Corresponding author. [Supplemental material is available online at www.genome.org.]
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