Role of MicroRNAs in Controlling Gene Expression in Different Segments of the Human Epididymis

被引:87
作者
Belleannee, Clemence [1 ,2 ]
Calvo, Ezequiel [3 ,4 ]
Thimon, Veronique
Cyr, Daniel G. [5 ]
Legare, Christine [1 ,2 ]
Garneau, Louis [1 ,2 ]
Sullivan, Robert [1 ,2 ,3 ,4 ]
机构
[1] Univ Laval, Ctr Rech CHUQ, Fac Med, Quebec City, PQ G1K 7P4, Canada
[2] Univ Laval, Fac Med, Dept Obstet Gynecol, Quebec City, PQ G1K 7P4, Canada
[3] Univ Laval, Dept Mol Med, Quebec City, PQ G1K 7P4, Canada
[4] Univ Laval, Lab Endocrinol & Gen, CHUL Res Ctr, Quebec City, PQ G1K 7P4, Canada
[5] Univ Quebec, Inst Armand Frappier, INRS, Laval, PQ, Canada
来源
PLOS ONE | 2012年 / 7卷 / 04期
基金
加拿大健康研究院;
关键词
LOOP RT-PCR; LUMINAL FLUID; PROTEINS; RNA; RAT; TRANSCRIPTOME; BARRIER; ADULT; IDENTIFICATION; SPERMATOZOA;
D O I
10.1371/journal.pone.0034996
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The molecular mechanisms implicated in regionalized gene expression in the human epididymis have not yet been fully elucidated. Interestingly, more than 200 microRNAs (miRNAs) have been identified in the human epididymis and could be involved in the regulation of mRNA stability and post-transcriptional expression in this organ. Methods: Using a miRNA microarray approach, we investigated the correlation between miRNA signatures and gene expression profiles found in three distinct regions (caput, corpus and cauda) of human epididymides from 3 donors. In silico prediction of transcript miRNA targets was performed using TargetScan and Miranda software's. FHCE1 immortalized epididymal cell lines were cotransfected with mimic microRNAs and plasmid constructs containing the 3'UTR of predicted target genes downstream of the luciferase gene. Results: We identified 35 miRNAs differentially expressed in the distinct segments of the epididymis (fold change >= 2, P-value <= 0.01). Among these miRNAs, miR-890, miR-892a, miR-892b, miR-891a, miR-891b belonging to the same epididymis-enriched cluster located on the X chromosome, are significantly more expressed in the corpus and cauda regions than in the caput. Interestingly, a strong negative correlation (r = -0,89, P-value <= 0.001) was found between the pattern of expression of miR-892b and its potential mRNA target Esrrg (Estrogen Related Receptor Gamma) and with miR-145 and Cldn10 mRNA (r = -0,92, P-value <= 0.001). We confirmed that miR-145 and miR-892b inhibit the expression of the luciferase reporter via Cldn10 and Esrrg 39 UTRs, respectively. Conclusion: Our study shows that the expression of miRNAs is segmented along the human epididymis and correlates with the pattern of target gene expression in different regions. Therefore, epididymal miRNAs may be in control of the maintenance of gene expression profile in the epididymis, which dictates segment-specific secretion of proteins and establishes physiological compartments that directly or indirectly affect sperm maturation and fertility.
引用
收藏
页数:13
相关论文
共 65 条
[1]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[2]   Micromanagers of gene expression: the potentially widespread influence of metazoan microRNAs [J].
Bartel, DP ;
Chen, CZ .
NATURE REVIEWS GENETICS, 2004, 5 (05) :396-400
[3]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[4]   Purification and identification of sperm surface proteins and changes during epididymal maturation [J].
Belleannee, Clemence ;
Belghazi, Maya ;
Labas, Valerie ;
Teixeira-Gomes, Ana-Paula ;
Gatti, Jean Luc ;
Dacheux, Jean-Louis ;
Dacheux, Francoise .
PROTEOMICS, 2011, 11 (10) :1952-1964
[5]   Identification of luminal and secreted proteins in bull epididymis [J].
Belleannee, Clemence ;
Labas, Valerie ;
Teixeira-Gomes, Ana-Paula ;
Gatti, Jean Luc ;
Dacheux, Jean-Louis ;
Dacheux, Francoise .
JOURNAL OF PROTEOMICS, 2011, 74 (01) :59-78
[6]   Esrrg functions in early branch generation of the ureteric bud and is essential for normal development of the renal papilla [J].
Berry, Rachel ;
Harewood, Louise ;
Pei, Liming ;
Fisher, Malcolm ;
Brownstein, David ;
Ross, Allyson ;
Alaynick, William A. ;
Moss, Julie ;
Hastie, Nicholas D. ;
Hohenstein, Peter ;
Davies, Jamie A. ;
Evans, Ronald M. ;
FitzPatrick, David R. .
HUMAN MOLECULAR GENETICS, 2011, 20 (05) :917-926
[7]   Profiling and imaging proteins in the mouse epididymis by imaging mass spectrometry [J].
Chaurand, P ;
Fouchécourt, S ;
DaGue, BB ;
Xu, BGJ ;
Reyzer, ML ;
Orgebin-Crist, MC ;
Caprioli, RM .
PROTEOMICS, 2003, 3 (11) :2221-2239
[8]   Real-time quantification of microRNAs by stem-loop RT-PCR [J].
Chen, CF ;
Ridzon, DA ;
Broomer, AJ ;
Zhou, ZH ;
Lee, DH ;
Nguyen, JT ;
Barbisin, M ;
Xu, NL ;
Mahuvakar, VR ;
Andersen, MR ;
Lao, KQ ;
Livak, KJ ;
Guegler, KJ .
NUCLEIC ACIDS RESEARCH, 2005, 33 (20) :e179.1-e179.9
[9]  
CORNWALL GA, 1995, J ANDROL, V16, P379
[10]   INTERACTIONS OF LABELED EPIDIDYMAL SECRETORY PROTEINS WITH SPERMATOZOA AFTER INJECTION OF S-35 METHIONINE IN THE MOUSE [J].
CORNWALL, GA ;
VREEBURG, JT ;
HOLLAND, MK ;
ORGEBINCRIST, MC .
BIOLOGY OF REPRODUCTION, 1990, 43 (01) :121-129