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Molecular cloning and evolutionary analysis of captive forest musk deer bitter taste receptor gene T2R16.

Authors :
Zhao GJ
Wu N
Li DY
Zeng DJ
Chen Q
Lu L
Feng XL
Zhang CL
Zheng CL
Jie H
Source :
Genetics and molecular research : GMR [Genet Mol Res] 2015 Dec 08; Vol. 14 (4), pp. 16185-95. Date of Electronic Publication: 2015 Dec 08.
Publication Year :
2015

Abstract

Sensing bitter tastes is crucial for most animals because it can prevent them from ingesting harmful food. This process is mainly mediated by the bitter taste receptors (T2R) that are largely expressed in the taste buds. Previous studies have identified some T2R gene repertoires. Marked variation in repertoire size has been noted among species. However, research on T2Rs is still limited and the mechanisms underlying the evolution of vertebrate T2Rs remain poorly understood. In the present study, we analyzed the structure and features of the protein encoded by the forest musk deer (Moschus berezovskii) T2R16 and submitted the gene sequence to NCBI GenBank. The results showed that the full coding DNA sequence (CDS) of musk deer T2R16 (GenBank accession No. KP677279) was 906 bp, encoding 301 amino acids, which contained ATG start codon and TGA stop codon, with a calculated molecular weight of 35.03 kDa and an isoelectric point of 9.56. The T2R16 protein receptor had seven conserved transmembrane regions. Hydrophobicity analysis showed that most amino acid residues in T2R16 protein were hydrophobic, and the grand average of hydrophobicity (GRAVY) was 0.657. Phylogenetic analysis based on this gene revealed that forest musk deer had the closest association with sheep (Ovis aries), as compared to cow (Bos taurus), Tursiops truncatus, and other species, whereas it was genetically farthest from humans (Homo sapiens). We hope these results would complement the existing data on T2R16 and encourage further research in this respect.

Details

Language :
English
ISSN :
1676-5680
Volume :
14
Issue :
4
Database :
MEDLINE
Journal :
Genetics and molecular research : GMR
Publication Type :
Academic Journal
Accession number :
26662411
Full Text :
https://doi.org/10.4238/2015.December.8.8