Regulation of rDNA transcription in response to growth factors, nutrients and energy

被引:80
作者
Kusnadi, Eric P. [1 ,2 ]
Hannan, Katherine M. [1 ,3 ]
Hicks, Rodney J. [1 ,2 ]
Hannan, Ross D. [1 ,2 ,3 ,4 ,5 ]
Pearson, Richard B. [1 ,2 ,3 ,4 ]
Kang, Jian [1 ]
机构
[1] Peter MacCallum Canc Ctr, Div Res, Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Dept Biochem & Mol Biol, Parkville, Vic 3052, Australia
[4] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3168, Australia
[5] Univ Queensland, Sch Biomed Sci, Brisbane, Qld 4072, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
rDNA transcription; mTORC1; Growth factors; Nutrients; Amino acids; Energy; RNA-POLYMERASE-I; ACTIVATED PROTEIN-KINASE; CANCER-SPECIFIC ACTIVATION; AMINO-ACID TRANSPORTERS; P70; S6; KINASE; C-MYC; GLUTAMINE-METABOLISM; RIBOSOMAL DNA; DEPENDENT REGULATION; MAMMALIAN TARGET;
D O I
10.1016/j.gene.2014.11.010
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Exquisite control of ribosome biogenesis is fundamental for the maintenance of cellular growth and proliferation. Importantly, synthesis of ribosomal RNA by RNA polymerase I is a key regulatory step in ribosome biogenesis and a major biosynthetic and energy consuming process. Consequently, ribosomal RNA gene transcription is tightly coupled to the availability of growth factors, nutrients and energy. Thus cells have developed an intricate sensing network to monitor the cellular environment and modulate ribosomal DNA transcription accordingly. Critical controllers in these sensing networks, which mediate growth factor activation of ribosomal DNA transcription, include the PI3K/AKT/mTORC1, RAS/RAF/ERK pathways and MYC transcription factor. mTORC1 also responds to amino acids and energy status, making it a key hub linking all three stimuli to the regulation of ribosomal DNA transcription, although this is achieved via overlapping and distinct mechanisms. This review outlines the current knowledge of how cells respond to environmental cues to control ribosomal RNA synthesis. We also highlight the critical points within this network that are providing new therapeutic opportunities for treating cancers through modulation of RNA polymerase I activity and potential novel imaging strategies. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:27 / 34
页数:8
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