Differential expression and emerging functions of non-coding RNAs in cold adaptation

被引:11
作者
Frigault, Jacques J. [1 ]
Morin, Mathieu D. [1 ]
Morin, Pier, Jr. [1 ]
机构
[1] Univ Moncton, Dept Chem & Biochem, 18 Antonine Maillet Ave, Moncton, NB E1A 3E9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Mammalian hibernation; Insect cold hardiness; Cold adaptation; Non-coding RNAs; MicroRNAs; Long non-coding RNAs; 13-LINED GROUND-SQUIRRELS; MYOCYTE ENHANCER FACTOR-2; METABOLIC-RATE DEPRESSION; FREEZE-TOLERANT INSECT; GENE-EXPRESSION; LOW-TEMPERATURE; MAMMALIAN HIBERNATION; MICRORNA EXPRESSION; DNA METHYLATION; REVERSIBLE PHOSPHORYLATION;
D O I
10.1007/s00360-016-1049-2
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Several species undergo substantial physiological and biochemical changes to confront the harsh conditions associated with winter. Small mammalian hibernators and cold-hardy insects are examples of natural models of cold adaptation that have been amply explored. While the molecular picture associated with cold adaptation has started to become clearer in recent years, notably through the use of high-throughput experimental approaches, the underlying cold-associated functions attributed to several non-coding RNAs, including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), remain to be better characterized. Nevertheless, key pioneering work has provided clues on the likely relevance of these molecules in cold adaptation. With an emphasis on mammalian hibernation and insect cold hardiness, this work first reviews various molecular changes documented so far in these processes. The cascades leading to miRNA and lncRNA production as well as the mechanisms of action of these non-coding RNAs are subsequently described. Finally, we present examples of differentially expressed non-coding RNAs in models of cold adaptation and elaborate on the potential significance of this modulation with respect to low-temperature adaptation.
引用
收藏
页码:19 / 28
页数:10
相关论文
共 95 条
[11]   Insight into post-transcriptional gene regulation: stress-responsive microRNAs and their role in the environmental stress survival of tolerant animals [J].
Biggar, Kyle K. ;
Storey, Kenneth B. .
JOURNAL OF EXPERIMENTAL BIOLOGY, 2015, 218 (09) :1281-1289
[12]   Identification and expression of microRNA in the brain of hibernating bats, Myotis lucifugus [J].
Biggar, Kyle K. ;
Storey, Kenneth B. .
GENE, 2014, 544 (01) :67-74
[13]  
Biggar Kyle K., 2012, Genomics Proteomics & Bioinformatics, V10, P302, DOI 10.1016/j.gpb.2012.09.002
[14]   Global DNA modifications suppress transcription in brown adipose tissue during hibernation [J].
Biggar, Yulia ;
Storey, Kenneth B. .
CRYOBIOLOGY, 2014, 69 (02) :333-338
[15]   GW182 Proteins Directly Recruit Cytoplasmic Deadenylase Complexes to miRNA Targets [J].
Braun, Joerg E. ;
Huntzinger, Eric ;
Fauser, Maria ;
Izaurralde, Elisa .
MOLECULAR CELL, 2011, 44 (01) :120-133
[16]   Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses [J].
Cabili, Moran N. ;
Trapnell, Cole ;
Goff, Loyal ;
Koziol, Magdalena ;
Tazon-Vega, Barbara ;
Regev, Aviv ;
Rinn, John L. .
GENES & DEVELOPMENT, 2011, 25 (18) :1915-1927
[17]   The long noncoding RNA TUG1 regulates blood-tumor barrier permeability by targeting miR-144 [J].
Cai, Heng ;
Xue, Yixue ;
Wang, Ping ;
Wang, Zhenhua ;
Li, Zhen ;
Hu, Yi ;
Li, Zhiqing ;
Shang, Xiuli ;
Liu, Yunhui .
ONCOTARGET, 2015, 6 (23) :19759-19779
[18]   The imprinted H19 noncoding RNA is a primary microRNA precursor [J].
Cai, Xuezhong ;
Cullen, Bryan R. .
RNA, 2007, 13 (03) :313-316
[19]   Mammalian hibernation: Cellular and molecular responses to depressed metabolism and low temperature [J].
Carey, HV ;
Andrews, MT ;
Martin, SL .
PHYSIOLOGICAL REVIEWS, 2003, 83 (04) :1153-1181
[20]   A Long Noncoding RNA Controls Muscle Differentiation by Functioning as a Competing Endogenous RNA [J].
Cesana, Marcella ;
Cacchiarelli, Davide ;
Legnini, Ivano ;
Santini, Tiziana ;
Sthandier, Olga ;
Chinappi, Mauro ;
Tramontano, Anna ;
Bozzoni, Irene .
CELL, 2011, 147 (02) :358-369