Genomic analysis of expressed sequence tags in American black bear Ursus americanus
- Equal contributors
1 CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes of Biological Sciences, 320 Yue Yang Road, Shanghai, 200031, China
2 Institute of Arctic Biology, University of Alaska Fairbanks, Fairbanks, AK, 99775, USA
3 Current address: Microbial Evolution Research Group (MERG), Department of Biology, University of Oslo, N-0316 Oslo, Norway
BMC Genomics 2010, 11:201 doi:10.1186/1471-2164-11-201Published: 26 March 2010
Species of the bear family (Ursidae) are important organisms for research in molecular evolution, comparative physiology and conservation biology, but relatively little genetic sequence information is available for this group. Here we report the development and analyses of the first large scale Expressed Sequence Tag (EST) resource for the American black bear (Ursus americanus).
Comprehensive analyses of molecular functions, alternative splicing, and tissue-specific expression of 38,757 black bear EST sequences were conducted using the dog genome as a reference. We identified 18 genes, involved in functions such as lipid catabolism, cell cycle, and vesicle-mediated transport, that are showing rapid evolution in the bear lineage Three genes, Phospholamban (PLN), cysteine glycine-rich protein 3 (CSRP3) and Troponin I type 3 (TNNI3), are related to heart contraction, and defects in these genes in humans lead to heart disease. Two genes, biphenyl hydrolase-like (BPHL) and CSRP3, contain positively selected sites in bear. Global analysis of evolution rates of hibernation-related genes in bear showed that they are largely conserved and slowly evolving genes, rather than novel and fast-evolving genes.
We provide a genomic resource for an important mammalian organism and our study sheds new light on the possible functions and evolution of bear genes.