Translation control of mRNAs encoding mammalian translation initiation factors

被引:11
作者
Andreev, Dmitri E. [1 ]
Dmitriev, Sergey E. [1 ,3 ]
Loughran, Gary [2 ]
Terenin, Ilya M. [1 ]
Baranov, Pavel V. [2 ]
Shatsky, Ivan N. [1 ]
机构
[1] Lomonosov Moscow State Univ, Belozersky Inst Physicochem Biol, Moscow, Russia
[2] Univ Coll Cork, Sch Biochem & Cell Biol, Cork, Ireland
[3] Lomonosov Moscow State Univ, Biol Fac, Dept Biochem, Moscow, Russia
基金
俄罗斯科学基金会;
关键词
mRNA; Translation initiation; uORF; TISU; IRES; Protein synthesis; Autoregulation; eIF; RIBOSOME ENTRY SITE; MODULATES AUTOREGULATION; PROTEIN-SYNTHESIS; FACTOR; 4GI; FACTOR IF3; CODON; EIF3; SUBUNITS; GENE; RECONSTITUTION;
D O I
10.1016/j.gene.2018.02.013
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Eukaryotic cells evolved highly complex and accurate protein synthesis machinery that is finely tuned by various signaling pathways. Dysregulation of translation is a hallmark of many diseases, including cancer, and thus pharmacological approaches to modulate translation become very promising. While there has been much progress in our understanding of mammalian mRNA-specific translation control, surprisingly, relatively little is known about whether and how the protein components of the translation machinery shape translation of their own mRNAs. Here we analyze mammalian mRNAs encoding components of the translation initiation machinery for potential regulatory features such as 5'TOP motifs, TISU motifs, poor start codon nucleotide context and upstream open reading frames.
引用
收藏
页码:174 / 182
页数:9
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