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Single-cell profiling reveals transcriptome dynamics during bovine oocyte growth.
Latorraca, Lais Barbosa; Galvão, António; Rabaglino, Maria Belen; D'Augero, Julieta Maria; Kelsey, Gavin; Fair, Trudee.
Afiliación
  • Latorraca LB; School of Agriculture and Food Science, University College Dublin, Dublin, Ireland.
  • Galvão A; Epigenetics Programme, The Babraham Institute, Cambridge, UK.
  • Rabaglino MB; Department of Comparative Biomedical Sciences, Royal Veterinary College, London, UK.
  • D'Augero JM; Department of Population Health Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 7, 3584 CL, Utrecht, The Netherlands.
  • Kelsey G; School of Agriculture and Food Science, University College Dublin, Dublin, Ireland.
  • Fair T; Epigenetics Programme, The Babraham Institute, Cambridge, UK.
BMC Genomics ; 25(1): 335, 2024 Apr 06.
Article en En | MEDLINE | ID: mdl-38580918
ABSTRACT

BACKGROUND:

Mammalian follicle development is characterized by extensive changes in morphology, endocrine responsiveness, and function, providing the optimum environment for oocyte growth, development, and resumption of meiosis. In cattle, the first signs of transcription activation in the oocyte are observed in the secondary follicle, later than during mouse and human oogenesis. While many studies have generated extensive datasets characterizing gene expression in bovine oocytes, they are mostly limited to the analysis of fully grown and matured oocytes. The aim of the present study was to apply single-cell RNA sequencing to interrogate the transcriptome of the growing bovine oocyte from the secondary follicle stage through to the mid-antral follicle stage.

RESULTS:

Single-cell RNA-seq libraries were generated from oocytes of known diameters (< 60 to > 120 µm), and datasets were binned into non-overlapping size groups for downstream analysis. Combining the results of weighted gene co-expression network and Trendy analyses, and differently expressed genes (DEGs) between size groups, we identified a decrease in oxidative phosphorylation and an increase in maternal -genes and transcription regulators across the bovine oocyte growth phase. In addition, around 5,000 genes did not change in expression, revealing a cohort of stable genes. An interesting switch in gene expression profile was noted in oocytes greater than 100 µm in diameter, when the expression of genes related to cytoplasmic activities was replaced by genes related to nuclear activities (e.g., chromosome segregation). The highest number of DEGs were detected in the comparison of oocytes 100-109 versus 110-119 µm in diameter, revealing a profound change in the molecular profile of oocytes at the end of their growth phase.

CONCLUSIONS:

The current study provides a unique dataset of the key genes and pathways characteristic of each stage of oocyte development, contributing an important resource for a greater understanding of bovine oogenesis.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oogénesis / Transcriptoma Límite: Animals / Female / Humans Idioma: En Revista: BMC Genomics Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article País de afiliación: Irlanda

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Oogénesis / Transcriptoma Límite: Animals / Female / Humans Idioma: En Revista: BMC Genomics Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article País de afiliación: Irlanda