Abstract

The aim of this study was to perform a proteomic analysis to isolate and identify proteins from the swine sperm nuclear matrix to contribute to a database of swine sperm nuclear proteins. We used prechilled diluted semen from seven boars (19 to 24 weekold) from the commercial line Landrace x Large White x Pietran. The semen was processed to separate the sperm heads and extract the chromatin and nuclear matrix for protein quantification and analysis by mass spectrometry, by LTQ Orbitrap ELITE mass spectrometer (Thermo-Finnigan) coupled to a nanoflow chromatography system (LC-MS/MS). We identified 222 different proteins in the sample; a total of 159 (71.6%) were previously described as present in the somatic or sperm nuclei of other species, 41 (18.5%) did not have a previously reported nuclear presence and 22 (9.9%) had not been characterized. The most abundant family of proteins corresponded to ribosomal (13.1%), followed by cytoskeleton (12.2%), uncharacterized (9.9%), histones (5.4%), proteasome subunits (3.6%) and heat shock (1.8%). The other proteins clustered in other families accounted for 54% of the total proteins. The protein isolation of the nuclear matrix of the swine spermatozoa was satisfactory, thus demonstrating that the protocol used was efficient. Several proteins were identified and described. However, it was not possible to identify some protein structures. Therefore, this study helps to establish a starting point for future proteomic studies comparing fertile and sub-fertile animals.

Highlights

  • It has long been thought that the only function of sperm cells is to transmit the paternal genomic DNA to the generation

  • The aim of this study was to perform a proteomic analysis to isolate and identify proteins from the swine sperm nuclear matrix to contribute to a database of swine sperm nuclear proteins

  • The results of toluidine blue analyses suggest that the animals in question presented normal sperm with respect to chromatin compaction (Beletti et al, 2005)

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Summary

Introduction

It has long been thought that the only function of sperm cells is to transmit the paternal genomic DNA to the generation. DNA condensation by sperm protamines leaves only a small fraction of the sperm genome accessible for DNA binding proteins, which are necessary to enable DNA replication and genes transcription. These sites may be the most important sites for the initiation of paternal genome functions in the early embryo. Prediluted (diluent BTS) and cooled boar semen was used in this study, with concentration of 2.5 x 109 (80 ml/dose). The breeders chosen were normally used by insemination center, where the resulting litters, borned to the date of collection, were within zootechnical levels proposed for the line in question

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