生物
重编程
肽
外显子
选择性拼接
细胞生物学
基因
遗传学
生物化学
作者
Jinzhou Huang,Min Chen,De Chen,Xing-Cheng Gao,Song Zhu,Hongyang Huang,Min Hu,Huifang Zhu,Guang‐Rong Yan
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2017-10-01
卷期号:68 (1): 171-184.e6
被引量:618
标识
DOI:10.1016/j.molcel.2017.09.015
摘要
A substantial fraction of eukaryotic transcripts are considered long non-coding RNAs (lncRNAs), which regulate various hallmarks of cancer. Here, we discovered that the lncRNA HOXB-AS3 encodes a conserved 53-aa peptide. The HOXB-AS3 peptide, not lncRNA, suppresses colon cancer (CRC) growth. Mechanistically, the HOXB-AS3 peptide competitively binds to the ariginine residues in RGG motif of hnRNP A1 and antagonizes the hnRNP A1-mediated regulation of pyruvate kinase M (PKM) splicing by blocking the binding of the ariginine residues in RGG motif of hnRNP A1 to the sequences flanking PKM exon 9, ensuring the formation of lower PKM2 and suppressing glucose metabolism reprogramming. CRC patients with low levels of HOXB-AS3 peptide have poorer prognoses. Our study indicates that the loss of HOXB-AS3 peptide is a critical oncogenic event in CRC metabolic reprogramming. Our findings uncover a complex regulatory mechanism of cancer metabolism reprogramming orchestrated by a peptide encoded by an lncRNA.
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