Molecular cloning and characterization of CD14 gene in goat

被引:9
|
作者
Pal, Aruna [1 ]
Chatterjee, P. N. [2 ]
机构
[1] Indian Vet Res Inst, Div Anim Genet, Izatnagar 243122, UP, India
[2] Indian Vet Res Inst, Anim Nutr Div, Izatnagar 243122, UP, India
关键词
Cloning; CD14; gene; Goat; Codon; Sequencing; LIPOPOLYSACCHARIDE; CELLS; NUCLEOTIDE; PROTEIN; BINDING; LPS;
D O I
10.1016/j.smallrumres.2008.11.016
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
The present study was carried out in the Animal Genetics Division, Indian Veterinary Research Institute. The cDNA for CD14 gene of goat was amplified for the first time using PCR with ATGGTCTGCGTGCCCTACCTG as forward primer and GGAGCCCGAGGCTTCGCGTAA as reverse primer. The PCR product of 1122 bp was eluted, purified, cloned and sequenced by automated sequencer (ABI prism) using dideoxy chain termination method. CD14 cDNA (Gene bank Accession no. DQ457090) revealed 1122 bp nucleotide with ATG as start codon followed by an open reading frame of 1116 nucleotides and TAA as stop codon. GC content of caprine CD14 gene was found to be as high as 62.21%. The predicted peptide sequence revealed 373 amino acids precursor corresponding to coding sequence of CD14 gene and a 20 amino acid signal peptide. Caprine CD14 peptide is of higher Mol wt. than buffalo, but lesser than cattle. Caprine CD14 cDNA gene is 92.0, 92.5, 75.7, 76.1, 69.2 and 61.7% identical to buffalo, cattle, human, dog, mouse and rat cDNA. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 87
页数:4
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