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LH/hCG Regulation of Circular RNA in Mural Granulosa Cells during the Periovulatory Period in Mice

Ovarian follicles undergo a series of dynamic changes following the ovulatory surge of luteinizing hormone including cumulus expansion, oocyte maturation, ovulation, and luteinization. Post-transcriptional gene regulatory events are critical for mediating LH follicular responses, and among all RNA i...

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Autores principales: Chakravarthi, V. Praveen, Hung, Wei-Ting, Yellapu, Nanda Kumar, Gunewardena, Sumedha, Christenson, Lane K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488058/
https://www.ncbi.nlm.nih.gov/pubmed/37685885
http://dx.doi.org/10.3390/ijms241713078
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author Chakravarthi, V. Praveen
Hung, Wei-Ting
Yellapu, Nanda Kumar
Gunewardena, Sumedha
Christenson, Lane K.
author_facet Chakravarthi, V. Praveen
Hung, Wei-Ting
Yellapu, Nanda Kumar
Gunewardena, Sumedha
Christenson, Lane K.
author_sort Chakravarthi, V. Praveen
collection PubMed
description Ovarian follicles undergo a series of dynamic changes following the ovulatory surge of luteinizing hormone including cumulus expansion, oocyte maturation, ovulation, and luteinization. Post-transcriptional gene regulatory events are critical for mediating LH follicular responses, and among all RNA isoforms, circular RNA (circRNA) is one of the most abundant forms present in cells, yet they remain the least studied. Functionally, circRNA can act as miRNA sponges, protein sponges/decoys, and regulators of transcription and translation. In the context of ovarian follicular development, the identity and roles of circRNA are relatively unknown. In the present study, high throughput RNA sequencing of granulosa cells immediately prior to and 4-h after the LH/hCG surge identified 42,381 circRNA originating from 7712 genes. A total of 54 circRNA were identified as differentially expressed between 0-h and 4-h time points (Fold Change ± 1.5, FDR ≤ 0.1), among them 42 circRNA were upregulated and 12 circRNA were downregulated. All differentially expressed circRNA between the 0-h and 4-h groups were subjected to circinteractome analysis and identified networks of circRNA-protein and circRNA-miRNA were further subjected to “micro-RNA target filter analysis” in Ingenuity Pathway Analyses, which resulted in the identification of miRNA targeted mRNAs. A comparison of these circRNA target mRNAs with LH-induced mRNAs identified Runx2, Egfr, Areg, Sult1el, Cyp19a1, Cyp11a1, and Hsd17b1 as targets of circKif2, circVcan, circMast4, and circMIIt10. These newly identified LH/hCG-induced circRNA, their target miRNA and protein networks provide new insights into the complex interactions associated with periovulatory follicular development.
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spelling pubmed-104880582023-09-09 LH/hCG Regulation of Circular RNA in Mural Granulosa Cells during the Periovulatory Period in Mice Chakravarthi, V. Praveen Hung, Wei-Ting Yellapu, Nanda Kumar Gunewardena, Sumedha Christenson, Lane K. Int J Mol Sci Article Ovarian follicles undergo a series of dynamic changes following the ovulatory surge of luteinizing hormone including cumulus expansion, oocyte maturation, ovulation, and luteinization. Post-transcriptional gene regulatory events are critical for mediating LH follicular responses, and among all RNA isoforms, circular RNA (circRNA) is one of the most abundant forms present in cells, yet they remain the least studied. Functionally, circRNA can act as miRNA sponges, protein sponges/decoys, and regulators of transcription and translation. In the context of ovarian follicular development, the identity and roles of circRNA are relatively unknown. In the present study, high throughput RNA sequencing of granulosa cells immediately prior to and 4-h after the LH/hCG surge identified 42,381 circRNA originating from 7712 genes. A total of 54 circRNA were identified as differentially expressed between 0-h and 4-h time points (Fold Change ± 1.5, FDR ≤ 0.1), among them 42 circRNA were upregulated and 12 circRNA were downregulated. All differentially expressed circRNA between the 0-h and 4-h groups were subjected to circinteractome analysis and identified networks of circRNA-protein and circRNA-miRNA were further subjected to “micro-RNA target filter analysis” in Ingenuity Pathway Analyses, which resulted in the identification of miRNA targeted mRNAs. A comparison of these circRNA target mRNAs with LH-induced mRNAs identified Runx2, Egfr, Areg, Sult1el, Cyp19a1, Cyp11a1, and Hsd17b1 as targets of circKif2, circVcan, circMast4, and circMIIt10. These newly identified LH/hCG-induced circRNA, their target miRNA and protein networks provide new insights into the complex interactions associated with periovulatory follicular development. MDPI 2023-08-23 /pmc/articles/PMC10488058/ /pubmed/37685885 http://dx.doi.org/10.3390/ijms241713078 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chakravarthi, V. Praveen
Hung, Wei-Ting
Yellapu, Nanda Kumar
Gunewardena, Sumedha
Christenson, Lane K.
LH/hCG Regulation of Circular RNA in Mural Granulosa Cells during the Periovulatory Period in Mice
title LH/hCG Regulation of Circular RNA in Mural Granulosa Cells during the Periovulatory Period in Mice
title_full LH/hCG Regulation of Circular RNA in Mural Granulosa Cells during the Periovulatory Period in Mice
title_fullStr LH/hCG Regulation of Circular RNA in Mural Granulosa Cells during the Periovulatory Period in Mice
title_full_unstemmed LH/hCG Regulation of Circular RNA in Mural Granulosa Cells during the Periovulatory Period in Mice
title_short LH/hCG Regulation of Circular RNA in Mural Granulosa Cells during the Periovulatory Period in Mice
title_sort lh/hcg regulation of circular rna in mural granulosa cells during the periovulatory period in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488058/
https://www.ncbi.nlm.nih.gov/pubmed/37685885
http://dx.doi.org/10.3390/ijms241713078
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