Reproduction  
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  

Reproduction (2009) 138 65-80
DOI: 10.1530/REP-08-0503
Copyright © 2009 Society for Reproduction and Fertility
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary Data
Right arrow All Versions of this Article:
138/1/65    most recent
REP-08-0503v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bissonnette, N.
Right arrow Articles by Boissonneault, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bissonnette, N.
Right arrow Articles by Boissonneault, G.

RESEARCH

Spermatozoal transcriptome profiling for bull sperm motility: a potential tool to evaluate semen quality

Nathalie Bissonnette1,2, Jean-Philippe Lévesque-Sergerie1,2, Catherine Thibault1 and Guylain Boissonneault2

1 Dairy and Swine Research and Development Center, Agriculture and Agri-Food Canada, 2000 College Road, Sherbrooke, Quebec, Canada J1M 1Z32 Université de Sherbrooke, Sherbrooke, Quebec, Canada J1H 5N4

Correspondence should be addressed to N Bissonnette at Dairy and Swine Research and Development Center, Agriculture and Agri-Food Canada; Email: nathalie.bissonnette{at}agr.gc.ca

Regarding bull fertility, establishing an association between in vitro findings and field fertility requires a multi-parametric approach that measures the integrity of various structures and dynamic functions, such as motion characteristics, among others. The heterogeneous RNA pattern of spermatozoa could be used in genomic analysis for evaluating both spermatogenesis and fertility potential of semen, mainly because of the static status of the transcriptome of this particular differentiated cell. In a previous study, we determined that some spermatozoal transcripts identified by PCR-based cDNA subtraction are associated with non-return rate, a field fertility index. In the present study, the microarray technology was used in conjunction with differential RNA transcript extraction. We have shown that among these genes, some transcripts are also associated with the motility status of a population of sperm cells fractionated from the same ejaculate. We highlighted a systematic data analysis and validation scheme important for the identification of significant transcripts in this context. With such an approach, we found that transcripts encoding a serine/threonine testis-specific protein kinase (TSSK6) and a metalloproteinase non coding RNA (ADAM5P) are associated with high-motility status (P<0.001), also confirmed by quantitative PCR (P=0.0075). This association was found only when transcripts were extracted using the hot-TRIzol protocol, whereas the cold-TRIzol RNA extract comprised mitochondrial transcripts. These results demonstrate that some transcripts previously identified in association with field fertility are also found associated with in vitro motility provided that a stringent RNA extraction protocol is used.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS  
Copyright © 2009 by the Society for Reproduction and Fertility.