Identification of novel and conserved microRNA and their expression in the gray mouse lemur, Microcebus murinus, a primate capable of daily torpor

被引:12
作者
Biggar, K. K. [1 ,2 ]
Luu, B. E. [1 ,2 ]
Wu, C. W. [1 ,2 ]
Pifferi, F. [3 ]
Perret, M. [3 ]
Storey, K. B. [1 ,2 ]
机构
[1] Carleton Univ, Inst Biochem, 1125 Colonel By Dr, Ottawa, ON K1S 5B6, Canada
[2] Carleton Univ, Dept Biol, 1125 Colonel By Dr, Ottawa, ON K1S 5B6, Canada
[3] MNHN Natl Museum Nat Hist, Dept Ecol & Biodivers Management, UMR CNRS Natl Ctr Sci Res 7179, Brunoy, France
基金
加拿大自然科学与工程研究理事会;
关键词
Metabolic rate depression; Torpor; Primate; Environmental adaptation; DIFFERENTIAL EXPRESSION; MAMMALIAN HIBERNATOR; MATURE MICRORNAS; GROUND-SQUIRRELS; RESPONSES; SURVIVAL; MIRNAS; BATS;
D O I
10.1016/j.gene.2018.08.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
MicroRNA (miRNA) are endogenous small noncoding RNA gene products, on average 22 nt long, that play important regulatory roles in mediating gene expression by binding to and targeting mRNAs for degradation or translational repression. In this paper we identify both novel and conserved miRNA sequences present in the genome of the gray mouse lemur, Microcebus marinus. In total, 122 conserved and 44 novel miRNA were identified with high confidence from the lemur genome (Mmur_2.0) and were used for expression analysis. All conserved and novel miRNA were subjected to relative quantification by RT-qPCR in liver samples from control and torpid lemurs. A total of 26 miRNA (16 conserved and 10 novel) showed increased levels during primate torpor, whereas 31 (30 conserved and 1 novel) decreased. Additional in silico mapping of the predicted mRNA targets of torpor-responsive mature miRNA suggested that miRNA that increased during torpor were collectively involved in cell development and survival pathways, while miRNA that decreased were enriched in targeting immune function. Overall, the study suggests new regulatory mechanisms of primate torpor via miRNA action.
引用
收藏
页码:332 / 339
页数:8
相关论文
共 36 条
[1]   Functional impact of microRNA regulation in models of extreme stress adaptation [J].
Biggar, Kyle K. ;
Storey, Kenneth B. .
JOURNAL OF MOLECULAR CELL BIOLOGY, 2018, 10 (02) :93-101
[2]   Primate Torpor: Regulation of Stress-activated Protein Kinases During Daily Torpor in the Gray Mouse Lemur, Microcebus murinus [J].
Biggar, Kyle K. ;
Wu, Cheng-Wei ;
Tessier, Shannon N. ;
Zhang, Jing ;
Pifferi, Fabien ;
Perret, Martine ;
Storey, Kenneth B. .
GENOMICS PROTEOMICS & BIOINFORMATICS, 2015, 13 (02) :81-90
[3]   Modulation of Gene Expression in Key Survival Pathways During Daily Torpor in the Gray Mouse Lemur, Microcebus murinus [J].
Biggar, Kyle K. ;
Wu, Cheng-Wei ;
Tessier, Shannon N. ;
Zhang, Jing ;
Pifferi, Fabien ;
Perret, Martine ;
Storey, Kenneth B. .
GENOMICS PROTEOMICS & BIOINFORMATICS, 2015, 13 (02) :111-118
[4]  
Biggar Kyle K, 2014, Temperature (Austin), V1, P84, DOI 10.4161/temp.29656
[5]   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
[6]   High-throughput amplification of mature microRNAs in uncharacterized animal models using polyadenylated RNA and stem-loop reverse transcription polymerase chain reaction [J].
Biggar, Kyle K. ;
Wu, Cheng-Wei ;
Storey, Kenneth B. .
ANALYTICAL BIOCHEMISTRY, 2014, 462 :32-34
[7]   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
[8]   Hibernation: the immune system at rest? [J].
Bouma, Hjalmar R. ;
Carey, Hannah V. ;
Kroese, Frans G. M. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2010, 88 (04) :619-624
[9]   Primate Torpor Expression: Ghost of the Climatic Past [J].
Dausmann, Kathrin H. ;
Warnecke, Lisa .
PHYSIOLOGY, 2016, 31 (06) :398-408
[10]   MicroRNAs as regulators of metabolic disease: pathophysiologic significance and emerging role as biomarkers and therapeutics [J].
Deiuliis, J. A. .
INTERNATIONAL JOURNAL OF OBESITY, 2016, 40 (01) :88-101