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部分肝切除术诱导的长链非编码RNA在肝脏再生过程中抑制肝细胞增殖。

Partial Hepatectomy Induced Long Noncoding RNA Inhibits Hepatocyte Proliferation during Liver Regeneration.

作者信息

Huang Lulu, Damle Sagar S, Booten Sheri, Singh Priyam, Sabripour Mahyar, Hsu Jeff, Jo Minji, Katz Melanie, Watt Andy, Hart Christopher E, Freier Susan M, Monia Brett P, Guo Shuling

机构信息

Department of Antisense Drug Discovery, Isis Pharmaceuticals Inc., Carlsbad, CA, 92010, United States of America.

出版信息

PLoS One. 2015 Jul 24;10(7):e0132798. doi: 10.1371/journal.pone.0132798. eCollection 2015.

Abstract

Liver regeneration after partial hepatectomy (PHx) is a complex and well-orchestrated biological process in which synchronized cell proliferation is induced in response to the loss of liver mass. To define long noncoding RNAs (lncRNAs) that participate in the regulation of liver regeneration, we performed microarray analysis and identified more than 400 lncRNAs exhibiting significantly altered expression. Of these, one lncRNA, LncPHx2 (Long noncoding RNA induced by PHx 2), was highly upregulated during liver regeneration. Depletion of LncPHx2 during liver regeneration using antisense oligonucleotides led to a transient increase in hepatocyte proliferation and more rapid liver regeneration. Gene expression analysis showed that LncPHx2 depletion resulted in upregulation of mRNAs encoding proteins known to promote cell proliferation, including MCM components, DNA polymerases, histone proteins, and transcription factors. LncPHx2 interacts with the mRNAs of MCM components, making it a candidate to regulate the expression of MCMs and other genes post-transcriptionally. Collectively, our data demonstrate that LncPHx2 is a key lncRNA that participates in a negative feedback loop modulating hepatocyte proliferation through RNA-RNA interactions.

摘要

部分肝切除术后的肝脏再生是一个复杂且精心编排的生物学过程,在此过程中,肝脏质量的损失会诱导细胞同步增殖。为了确定参与肝脏再生调控的长链非编码RNA(lncRNA),我们进行了微阵列分析,并鉴定出400多个表达发生显著变化的lncRNA。其中,一种lncRNA,即LncPHx2(部分肝切除诱导的长链非编码RNA 2),在肝脏再生过程中高度上调。在肝脏再生过程中使用反义寡核苷酸耗尽LncPHx2会导致肝细胞增殖短暂增加以及肝脏再生加快。基因表达分析表明,LncPHx2的耗尽导致编码已知促进细胞增殖的蛋白质的mRNA上调,这些蛋白质包括微小染色体维持蛋白(MCM)组分、DNA聚合酶、组蛋白和转录因子。LncPHx2与MCM组分的mRNA相互作用,使其成为转录后调控MCM和其他基因表达的候选分子。总体而言,我们的数据表明,LncPHx2是一种关键的lncRNA,它通过RNA-RNA相互作用参与负反馈回路调节肝细胞增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cb2/4514479/c1e9d3a33208/pone.0132798.g001.jpg

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