Bioinformatics Analysis of JAZF1 Gene in Broilers
with Ascites Syndrome
FengPing Guo1§, Pei Liu1§,
Xiaoquan Guo1, Guyue Li1, Sufang Cheng2,
Zhenxing Zou3,
Xiaolu Hou4,
Vincent Latigo1, Lin Li1,
Guoliang Hu1* and Ping Liu1*
1Jiangxi
Provincial Key Laboratory for Animal Health, Institute of Animal
Population Health, College of Animal Science and Technology, Jiangxi
Agricultural University, Nanchang, Jiangxi 330045, China;
2Jiangxi
Biological Vocational College Nanchang jiangxi 330200 China; 3Hunan
Environmental Biological Vocational and Technical College, Hengyang
421005, China; 4Guangxi Agricultural Vocational College,
Nanning Guangxi 530007, China §The
authors contributed equally to this work.
*Corresponding author:
pingliujx@163.com;
hgljx@163.com
Abstract
Pulmonary vascular remodeling (PVR) is the main
characteristic lesion of ascites syndrome (AS) in broilers. JAZF1 plays an
important role in PVR, but there is no study on its protein function and
structure. In this study, the physical and chemical properties, hydrophilicity/hydrophobicity
and transmembrane domain, phosphorylation site and glycosylation site,
subcellular localization and signal peptide, secondary and tertiary structure,
antigen peptide and conserved domain and phylogenetic relationship of JAZF1
protein were predicted online by bioinformatics tools. The results showed that
the number of amino acids of JAZF1 was 243aa, the theoretical isoelectric point
was 8.63, the instability index was 58.1, and the average coefficient of
hydrophilicity was -0.674. It was found to be a hydrophilic protein having 35
phosphorylation sites and a N-glycosylation site with no transmembrane domain.
The protein is expressed in the nucleus, there is no signal peptide distribution
in the whole sequence and the secondary structure is mainly composed of random
coil and α- helix. There were 7 B cell epitopes, 7 conserved domains and
compared with other birds, JAZF1 is 95.61% similar. In summary, from the
analysis we came to conclude that the amino acid sequence 64-80aa, 91-108aa,
136-151aa and 179-187aa can be selected as antigen sites and among which
136-151aa may be the best. This study lays a good foundation for follow-up
experiments, which then provides powerful conditions for pathological detection
of pulmonary vascular remodeling and gene drug therapy of ascites syndrome in
broilers.
To Cite This Article: Guo FP, Liu P, Guo X, Li G, Cheng S, Zou Z, Hou
X, Latigo V, Li L, Hu GL and Liu P, 2021. Bioinformatics analysis of JAZF1 gene
in broilers with ascites syndrome. Pak Vet J, 41(1): 19-24. http://dx.doi.org/10.29261/pakvetj/2020.072