Title :
cDNA, Genomic Sequence Cloning and Sequence Analysis of Heat Shock Protein Beta-1 Gene (HSPB1) from the Giant Panda (Ailuropoda melanoleuca)
Author :
Song, Yan ; Hou, Yi-ling ; Hou, Wan-ru ; Wu, Guang-fu ; Zhang, Tian
Author_Institution :
Coll. of Life Sci., China West Normal Univ., Nanchong, China
Abstract :
The HSPB1´ office full name is heat shock protein beta-1, which is well-defined as a stress-inducible protein. It is a significant and interesting work to study it . The cDNA and the genomic sequence of HSPB1 was cloned successfully from the Giant Panda (Ailuropoda melanoleuca) using RT-PCR technology and touchdown-PCR, respectively, Both sequences were sequenced and analyzed preliminarily. The cDNA of the HSPB1 cloned from Giant Panda is 633bp in size, containing an open reading frame (ORF) of 624bp encoding 207 amino acids. The length of the genomic sequence is 1193 bp, which was found to possess three exons and two introns. Alignment analysis indicates that the nucleotide sequence of the coding sequence shows a high homology to those of Homo sapiens, Mus musculus, Bos Taurus, Canis lupus familiaris, Rattus norvegicus and Equus caballus are 89%, 85%, 88%, 93%, 83% and 91%, respectively . The homologies for deduced amino acid sequence are 89%, 90%, 90%, 92%, 88% and 92%, respectively. Topology prediction shows there are two N-myristoylation sites, four Protein kinase C phosphorylation sites, one Tyrosine kinase phosphorylation site, one cAMP- and cGMP-dependent protein kinase phosphorylation site and a ATP/GTP-binding site motif A (P-loop) in the HSPB1 protein of the Giant Panda. Futher analysis indicates that the expression sequence of HSPB1and the protein encoded are highly homologous to those of human and other mammals reported.
Keywords :
DNA; biochemistry; cellular biophysics; enzymes; genetic engineering; genetics; genomics; proteomics; zoology; ATP-GTP-binding site motif A; Ailuropoda melanoleuca; Bos Taurus; Canis lupus familiaris; Equus caballus; HSPB1; Homo sapiens; Mus musculus; N-myristoylation sites; RT-PCR technology; Rattus norvegicus; alignment analysis; amino acid sequence; amino acids; cAMP-dependent protein kinase phosphorylation site; cDNA; cGMP-dependent protein kinase phosphorylation site; exons; genomic sequence cloning; giant panda; heat shock protein beta-1 gene; homology; human; introns; mammals; protein kinase C phosphorylation sites; sequence analysis; touchdown-PCR; tyrosine kinase phosphorylation site; Amino acids; Bioinformatics; Cloning; Electric shock; Genomics; Humans; Muscles; Proteins; RNA; Sequences;
Conference_Titel :
Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
Conference_Location :
Chengdu
Print_ISBN :
978-1-4244-4712-1
Electronic_ISBN :
2151-7614
DOI :
10.1109/ICBBE.2010.5517383