Potential role of chimeric genes in pathway-related gene co-expression modules.
Potential role of chimeric genes in pathway-related gene co-expression modules.
复制标题
嵌合基因在通路相关基因共表达模块中的潜在作用
DOI:
10.1186/s12957-021-02248-9
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发表时间:
2021-05-12
影响因子:
3.2
通讯作者:
Ma L
中科院分区:
文献类型:
--
作者:
Li P;Li Y;Ma L
Gene fusion has epigenetic modification functions. The novel proteins encoded by gene fusion products play a role in cancer development. Therefore, a better understanding of the novel protein products may provide insights into the pathogenesis of tumors. However, the characteristics of chimeric genes are rarely studied. Here, we used weighted co-expression network analysis to investigate the biological roles and underlying mechanisms of chimeric genes. Download the pig transcriptome data, we screened chimeric genes and parental genes from 688 sequences and 153 samples, predict their domains, and analyze their associations. We constructed a co-expression network of chimeric genes in pigs and conducted Gene Ontology enrichment and Kyoto Encyclopedia of Genes and Genomes pathway analysis on the generated modules using DAVID to identify key networks and modules related to chimeric genes. Our findings showed that most of the protein domains of chimeric genes were derived from fused pre-genes. Chimeric genes were enriched in modules involved in the negative regulation of cell proliferation and protein localization to centrosomes. In addition, the chimeric genes were related to the growth factor-β superfamily, which regulates cell growth and differentiation. Furthermore, in helper T cells, chimeric genes regulate the specific recognition of T cell receptors, implying that chimeric genes play a key role in the regulation pathway of T cells. Chimeric genes can produce new domains, and some chimeric genes are a key role involved in pathway-related function. Most chimeric genes show binding activity. Domains of chimeric genes are derived from several combinations of parent genes. Chimeric genes play a key role in the regulation of several cellular pathways. Our findings may provide new directions to explore the roles of chimeric genes in tumors. The online version contains supplementary material available at 10.1186/s12957-021-02248-9.
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DOI:
10.3390/molecules23112798
发表时间:
2018-10-28
期刊:
Molecules (Basel, Switzerland)
影响因子:
--
作者:
Nguyen TH;Barr FG
通讯作者:
Barr FG
影响因子:
3
作者:
Langfelder P;Horvath S
通讯作者:
Horvath S
影响因子:
14.9
作者:
Kodama Y;Shumway M;Leinonen R;International Nucleotide Sequence Database Collaboration
通讯作者:
International Nucleotide Sequence Database Collaboration
DOI:
10.1093/bioinformatics/bts251
发表时间:
2012-07-01
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Jiao X;Sherman BT;Huang da W;Stephens R;Baseler MW;Lane HC;Lempicki RA
通讯作者:
Lempicki RA
影响因子:
3.5
作者:
Babteen, Nouf Abubakr;Fawzy, Manal S.;Elshazli, Rami M.
通讯作者:
Elshazli, Rami M.