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dc.rights.licenseReconocimiento 4.0 Internacional. (CC BY)-
dc.contributor.authorRomeo-Cardeillac, Carloses
dc.contributor.authorTrovero, María Fernandaes
dc.contributor.authorRadío, Santiagoes
dc.contributor.authorSmircich, Pabloes
dc.contributor.authorRodríguez-Casuriaga, Rosanaes
dc.contributor.authorGeisinger, Adrianaes
dc.contributor.authorSotelo-Silveira Josées
dc.date.accessioned2026-05-05T16:31:03Z-
dc.date.available2026-05-05T16:31:03Z-
dc.date.issued2024-03-20-
dc.identifier.urihttps://hdl.handle.net/20.500.12381/5518-
dc.description.abstractfrom spermatogenic cells, is reflected at the transcriptional level, with the largest number of tissue-specific genes and long noncoding RNAs (lncRNAs) compared to other tissues, and one of the highest rates of alternative splicing. Although it is known that adequate alternative-splicing patterns and stage-specific isoforms are critical for successful spermatogenesis, so far only a very limited number of reports have addressed a detailed study of alternative splicing and isoforms along the different spermatogenic stages. Results In the present work, using highly purified stage-specific testicular cell populations, we detected 33,002 transcripts expressed throughout mouse spermatogenesis not annotated so far. These include both splice variants of already annotated genes, and of hitherto unannotated genes. Using conservative criteria, we uncovered 13,471 spermatogenic lncRNAs, which reflects the still incomplete annotation of lncRNAs. A distinctive feature of lncRNAs was their lower number of splice variants compared to protein-coding ones, adding to the conclusion that lncRNAs are, in general, less complex than mRNAs. Besides, we identified 2,794 unannotated transcripts with high coding potential (including some arising from yet unannotated genes), many of which encode unnoticed putative testisspecific proteins. Some of the most interesting coding splice variants were chosen, and validated through RT-PCR. Remarkably, the largest number of stage-specific unannotated transcripts are expressed during early meiotic prophase stages, whose study has been scarcely addressed in former transcriptomic analyses. Conclusions We detected a high number of yet unannotated genes and alternatively spliced transcripts along mouse spermatogenesis, hence showing that the transcriptomic diversity of the testis is considerably higher than previously reported. This is especially prominent for specific, underrepresented stages such as those of early meiotic prophase, and its unveiling may constitute a step towards the understanding of their key events.es
dc.description.sponsorshipAgencia Nacional de Investigación e Innovaciónes
dc.description.sponsorshipComisión Sectorial Investigación Científica (CSIC, UdelaR)es
dc.language.isoenges
dc.publisherBMCes
dc.rightsAcceso abierto*
dc.sourceBMC Genomicses
dc.subjectmeiosises
dc.subjectspermatogenesises
dc.subjecttranscriptomicses
dc.subjectalternative splicinges
dc.subjectlncRNAses
dc.titleUncovering a multitude of stage-specific splice variants and putative protein isoforms generated along mouse spermatogenesises
dc.typeArtículoes
dc.subject.aniiCiencias Naturales y Exactas
dc.subject.aniiCiencias Biológicas
dc.subject.aniiBiología Reproductiva
dc.subject.aniiBioquímica y Biología Molecular
dc.identifier.aniiFCE_1_2021_1_166510es
dc.type.versionPublicadoes
dc.identifier.doi10.1186/s12864-024-10170-z-
dc.anii.institucionresponsableInstituto de Investigaciones Biológicas Clemente Establees
dc.anii.institucionresponsableFacultad de Ciencias (UdelaR)es
dc.anii.subjectcompleto//Ciencias Naturales y Exactas/Ciencias Biológicas/Biología Reproductivaes
dc.anii.subjectcompleto//Ciencias Naturales y Exactas/Ciencias Biológicas/Bioquímica y Biología Moleculares
Aparece en las colecciones: Instituto de Investigaciones Biológicas Clemente Estable

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