Selected article for: "acceptor site donor and donor acceptor"

Author: Liu, Xiaoping; Wang, Hanzhong; Liu, Xiaoqian; Li, Yong; Chen, Jing; Zhang, Jun; Wang, Xi; Shen, Shu; Wang, Hualin; Deng, Fei; Wang, Manli; Guan, Wuxiang; Hu, Zhihong
Title: Genomic and transcriptional analyses of novel parvoviruses identified from dead peafowl.
  • Cord-id: 32t0l8ko
  • Document date: 2019_10_31
  • ID: 32t0l8ko
    Snippet: To identify potential pathogens responsible for a disease outbreak of cultured peafowls in China in 2013, metagenomic sequencing was conducted. The genomes of two closely related parvoviruses, namely peafowl parvovirus 1 (PePV1) and PePV2, were identified with size of 4428 bp and 4348 bp, respectively. Phylogenetic analysis revealed that both viruses are novel parvoviruses, belonging to the proposed genus Chapparvovirus of Parvoviridae. The transcriptional profile of PePV1 was analyzed by transf
    Document: To identify potential pathogens responsible for a disease outbreak of cultured peafowls in China in 2013, metagenomic sequencing was conducted. The genomes of two closely related parvoviruses, namely peafowl parvovirus 1 (PePV1) and PePV2, were identified with size of 4428 bp and 4348 bp, respectively. Phylogenetic analysis revealed that both viruses are novel parvoviruses, belonging to the proposed genus Chapparvovirus of Parvoviridae. The transcriptional profile of PePV1 was analyzed by transfecting a nearly complete PePV1 genome into HEK-293T cells. Results revealed that PePV1 employs one promoter and two polyadenylation sites to start and terminate its transcriptions, with one donor site and two acceptor sites for pre-mRNA splicing. PePV1 DNA and structural protein were detected in several tissues of a dead peafowl, which appeared to have suffered enteritis, pneumonia and viremia. These results provide novel information of chapparvoviruses, and call for attention to the potential pathogens.

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