<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Wang X</submitter><pubmed_abstract>MicroRNAs regulate post-transcriptional gene expression via either translational repression or mRNA degradation. They have important roles in both viral infection and host anti-infection processes. We discovered that the miR-375 is significantly upregulated in Newcastle disease virus (NDV)-infected chicken embryonic visceral tissues using a small RNA sequencing approach. Further research revealed that the overexpression of miR-375 markedly decreases the replication of the velogenic NDV F48E9 and the lentogenic NDV La Sota by targeting the M gene of NDV in DF-1 cells. Interestingly, miR-375 has another target, ELAVL4, which regulates chicken fibrocyte cell cycle progression and decreases NDV proliferation. In addition, miR-375 can influence bystander cells by its secretion in culture medium</pubmed_abstract><journal>International journal of biological sciences</journal><pagination>44-57</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6329920</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MiR-375 Has Contrasting Effects on Newcastle Disease Virus Growth Depending on the Target Gene.</pubmed_title><pmcid>PMC6329920</pmcid><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Han Q</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Jia Y</pubmed_authors><pubmed_authors>Lv C</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Chu Z</pubmed_authors><pubmed_authors>Zhang S</pubmed_authors><pubmed_authors>Xiao S</pubmed_authors></additional><is_claimable>false</is_claimable><name>MiR-375 Has Contrasting Effects on Newcastle Disease Virus Growth Depending on the Target Gene.</name><description>MicroRNAs regulate post-transcriptional gene expression via either translational repression or mRNA degradation. They have important roles in both viral infection and host anti-infection processes. We discovered that the miR-375 is significantly upregulated in Newcastle disease virus (NDV)-infected chicken embryonic visceral tissues using a small RNA sequencing approach. Further research revealed that the overexpression of miR-375 markedly decreases the replication of the velogenic NDV F48E9 and the lentogenic NDV La Sota by targeting the M gene of NDV in DF-1 cells. Interestingly, miR-375 has another target, ELAVL4, which regulates chicken fibrocyte cell cycle progression and decreases NDV proliferation. In addition, miR-375 can influence bystander cells by its secretion in culture medium</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-05-06T21:04:19.763Z</modification><creation>2019-03-26T22:37:53Z</creation></dates><accession>S-EPMC6329920</accession><cross_references><pubmed>30662346</pubmed><doi>10.7150/ijbs.25106</doi></cross_references></HashMap>