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Sperm long non-coding RNAs as markers for ram fertility

dc.contributor.authorMustafa Hitit
dc.contributor.authorMustafa Hitit
dc.contributor.authorAbdullah Kaya
dc.contributor.authorErdogan Memili
dc.date.accessioned2026-01-04T20:24:22Z
dc.date.issued2024-05-10
dc.description.abstractIt is critical in sheep farming to accurately estimate ram fertility for maintaining reproductive effectiveness and for production profitability. However, there is currently a lack of reliable biomarkers to estimate semen quality and ram fertility, which is hindering advances in animal science and technology. The objective of this study was to uncover long non-coding RNAs (lncRNAs) in sperm from rams with distinct fertility phenotypes. Mature rams were allocated into two groups: high and low fertility (HF; n = 31; 94.5 ± 2.8%, LF; n = 25; 83.1 ± 5.73%; P = 0.028) according to the pregnancy rates sired by the rams (average pregnancy rate; 89.4 ± 7.2%). Total RNAs were isolated from sperm of the highest- and lowest-fertility rams (n = 4, pregnancy rate; 99.2 ± 1.6%, and 73.6 ± 4.4%, respectively) followed by next-generation sequencing of the transcripts. We uncovered 11,209 lncRNAs from the sperm of rams with HF and LF. In comparison to each other, there were 93 differentially expressed (DE) lncRNAs in sperm from the two distinct fertility phenotypes. Of these, 141 mRNAs were upregulated and 134 were downregulated between HF and LF, respectively. Genes commonly enriched for 9 + 2 motile cilium and sperm flagellum were ABHD2, AK1, CABS1, ROPN1, SEPTIN2, SLIRP, and TEKT3. Moreover, CABS1, CCDC39, CFAP97D1, ROPN1, SLIRP, TEKT3, and TTC12 were commonly enriched in flagellated sperm motility and sperm motility. Differentially expressed mRNAs were enriched in the top 16 KEGG pathways. Targets of the differentially expressed lncRNAs elucidate functions in cis and trans manner using the genetic context of the lncRNA locus, and lncRNA sequences revealed 471 mRNAs targets of 10 lncRNAs. This study illustrates the existence of potential lncRNA biomarkers that can be implemented in analyzing the quality of ram sperm and determining the sperm fertility and is used in breeding soundness exams for precision livestock farming to ensure food security on a global scale.
dc.description.urihttps://doi.org/10.3389/fvets.2024.1337939
dc.description.urihttps://pubmed.ncbi.nlm.nih.gov/38799722
dc.description.urihttp://dx.doi.org/10.3389/fvets.2024.1337939
dc.description.urihttps://doaj.org/article/1e307443e2994fad9d7e11b37609e2a0
dc.description.urihttps://aperta.ulakbim.gov.tr/record/277727
dc.identifier.doi10.3389/fvets.2024.1337939
dc.identifier.eissn2297-1769
dc.identifier.openairedoi_dedup___::25cfc7ea5e6bb3ba90e5ef93be68aede
dc.identifier.pubmed38799722
dc.identifier.scopus2-s2.0-85194137134
dc.identifier.urihttps://hdl.handle.net/20.500.12597/41781
dc.identifier.volume11
dc.identifier.wos001230145000001
dc.publisherFrontiers Media SA
dc.relation.ispartofFrontiers in Veterinary Science
dc.rightsOPEN
dc.subjectram
dc.subjectfertility
dc.subjectlong non-coding RNAs
dc.subjectVeterinary medicine
dc.subjectSF600-1100
dc.subjectgene expression
dc.subjectVeterinary Science
dc.subjectsperm
dc.subject.sdg2. Zero hunger
dc.titleSperm long non-coding RNAs as markers for ram fertility
dc.typeArticle
dspace.entity.typePublication
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However, there is currently a lack of reliable biomarkers to estimate semen quality and ram fertility, which is hindering advances in animal science and technology. The objective of this study was to uncover long non-coding RNAs (lncRNAs) in sperm from rams with distinct fertility phenotypes. Mature rams were allocated into two groups: high and low fertility (HF; <jats:italic>n</jats:italic> = 31; 94.5 ± 2.8%, LF; <jats:italic>n</jats:italic> = 25; 83.1 ± 5.73%; <jats:italic>P</jats:italic> = 0.028) according to the pregnancy rates sired by the rams (average pregnancy rate; 89.4 ± 7.2%). Total RNAs were isolated from sperm of the highest- and lowest-fertility rams (<jats:italic>n</jats:italic> = 4, pregnancy rate; 99.2 ± 1.6%, and 73.6 ± 4.4%, respectively) followed by next-generation sequencing of the transcripts. We uncovered 11,209 lncRNAs from the sperm of rams with HF and LF. In comparison to each other, there were 93 differentially expressed (DE) lncRNAs in sperm from the two distinct fertility phenotypes. Of these, 141 mRNAs were upregulated and 134 were downregulated between HF and LF, respectively. Genes commonly enriched for 9 + 2 motile cilium and sperm flagellum were <jats:italic>ABHD2, AK1, CABS1, ROPN1, SEPTIN2, SLIRP</jats:italic>, and <jats:italic>TEKT3</jats:italic>. Moreover, <jats:italic>CABS1, CCDC39, CFAP97D1, ROPN1, SLIRP, TEKT3</jats:italic>, and <jats:italic>TTC12</jats:italic> were commonly enriched in flagellated sperm motility and sperm motility. Differentially expressed mRNAs were enriched in the top 16 KEGG pathways. Targets of the differentially expressed lncRNAs elucidate functions in <jats:italic>cis</jats:italic> and <jats:italic>trans</jats:italic> manner using the genetic context of the lncRNA locus, and lncRNA sequences revealed 471 mRNAs targets of 10 lncRNAs. 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