Objective: To obtain the functional information of AY358935 gene.
Methods: The properties, subcellular location, and structure of AY358935 protein, and the expression profile of AY358935 gene were analyzed by bioinformatics software and the biological functions of the gene were predicted. AY358935 expression was detected by Western blot analysis in early virus infection.
Results: AY358935 was evolutionally conserved. The human AY358935 protein had an amino acid similarity of 74%, 60%, 38% and 33% with its counterpart in horses, mice, zebrafish and Xenopus laevis, respectively. Bioinformatics analysis indicated that AY358935 protein was located likely in the mitochondria. There was a N-terminal signal peptide and single transmembrane structure in AY358935 protein, which contained several phosphorylation sites. The secondary structure mainly comprised of alpha helices and random coils. AY358935 was ubiquitously expressed in normal tissues and carcinomas and regulated by the expression of double-stranded RNA-dependent protein kinase. AY358935 protein expression was obviously upregulated in cells 2 h after infection by vesicular stomatitis virus.
Conclusion: As a predicted secretary protein with a small molecular weight, AY358935 might have important functions in cellular proliferation and anti-viral innate immune regulation.
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Sichuan Da Xue Xue Bao Yi Xue Ban
July 2019
Department of Oncology, Affiliated Hospital of Chengdu University of TCM, Chengdu 610072, China.
Objective: To explore the anti-virus effect of 358935 gene cloned by our research team on vesicular stomatitis virus (VSV), and studytheanti-virus mechanism.
Methods: HEK293 cells were stably transfected by the 358935 gene recombinant plasmid pcDNA3.1-358935 or pcDNA3.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
June 2018
Department of Oncology, the Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610075, China.
Objective: To construct an eukaryotic expression plasmid for AY358935 gene and explore its function.
Methods: cDNA of the AY358935 gene was amplified by reverse transcription-PCR and cloned into pGEM-Teasy. The pGEM-T-AY was validated by sequencing and served as a template for the construction of eukaryotic expression plasmid.
Nan Fang Yi Ke Da Xue Xue Bao
February 2010
Department of Oncology, First Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine, Guangzhou 510405, China.
Objective: To obtain the functional information of AY358935 gene.
Methods: The properties, subcellular location, and structure of AY358935 protein, and the expression profile of AY358935 gene were analyzed by bioinformatics software and the biological functions of the gene were predicted. AY358935 expression was detected by Western blot analysis in early virus infection.
Genome Res
October 2003
Departments of Bioinformatics, Molecular Biology and Protein Chemistry, Genentech, Inc, South San Francisco, California 94080, USA.
A large-scale effort, termed the Secreted Protein Discovery Initiative (SPDI), was undertaken to identify novel secreted and transmembrane proteins. In the first of several approaches, a biological signal sequence trap in yeast cells was utilized to identify cDNA clones encoding putative secreted proteins. A second strategy utilized various algorithms that recognize features such as the hydrophobic properties of signal sequences to identify putative proteins encoded by expressed sequence tags (ESTs) from human cDNA libraries.
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