Expression of TXNRD1, HSPA4L and ATP1B1 Genes Associated with the Freezability of Boar Sperm

• Published in: International journal of molecular sciences 2022-08, Vol.23 (16), p.9320
• Main Authors: Mańkowska, Anna, Gilun, Przemysław, Zasiadczyk, Łukasz, Sobiech, Przemysław, Fraser, Leyland
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; ATP1B1 gene; Cold tolerance; Cryopreservation; Cryopreservation - methods; Densitometers; Fertility; Gel electrophoresis; Gene expression; Genes; Heat shock proteins; Hsp70 protein; Male; Motility; Oxidative stress; Protein expression; Reductases; RNA, Messenger - genetics; RNA, Messenger - metabolism; Semen; Semen Preservation - methods; Sperm; Sperm Motility - genetics; Spermatogenesis; Spermatozoa - metabolism; Swine; Thioredoxin; Thioredoxin Reductase 1 - metabolism; Western blotting
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23169320

Cryopreservation is associated with increased oxidative stress, which is responsible for sperm damage. We analyzed the effect of cryopreservation on mRNA and protein expression of thioredoxin reductase 1 ( ), heat shock protein family A (HSP 70) member 4 like ( ) and sodium/potassium-transporting ATPase subunit beta-1 ( ) genes in boar sperm with different freezability. Boars were classified as having good and poor semen freezability (GSF and PSF, respectively), according to the assessment of post-thaw sperm motility. Total RNA was isolated from fresh pre-freeze (PF) and frozen-thawed (FT) sperm from five boars of the GSF and PSF groups, respectively. Quantification of , and gene expression was performed by RT-qPCR analysis. Proteins extracted from sperm were subjected to Western blotting and SDS-PAGE analyses. Poor freezability ejaculates were characterized by significantly higher relative mRNA expression levels of and in FT sperm compared with the fresh PF sperm. Furthermore, the relative mRNA expression level of was significantly higher in the fresh PF sperm of the GSF group. Western blotting analysis revealed significantly higher relative expression of TXNRD1 protein in the fresh PF sperm of the GSF group, while HSPA4L protein expression was markedly increased in FT sperm of the PSF group. Electrophoretic and densitometric analyses revealed a higher number of proteins in the fresh PF and FT sperm of the PSF and GSF groups, respectively. The results of this study indicate that mRNA expression in the fresh PF sperm is a promising cryotolerance marker, while the variations of TXNRD1 and HSPA4L protein expression in the fresh PF or FT sperm provide useful information that may help to elucidate their biological significance in cryo-damage.