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Retinoblastoma binding protein 7 is involved in Kiss1 mRNA upregulation in rodents
Kisspeptin, encoded by Kiss1, is essential for reproduction in mammals. Kiss1 expression is regulated by estrogen via histone acetylation in the Kiss1 promotor region. Thus, elucidation of histone modification factor(s) involved in the regulation of Kiss1 expression is required to gain further under...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Society for Reproduction and Development
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175387/ https://www.ncbi.nlm.nih.gov/pubmed/31956172 http://dx.doi.org/10.1262/jrd.2019-149 |
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author | HORIHATA, Kei INOUE, Naoko UENOYAMA, Yoshihisa MAEDA, Kei-ichiro TSUKAMURA, Hiroko |
author_facet | HORIHATA, Kei INOUE, Naoko UENOYAMA, Yoshihisa MAEDA, Kei-ichiro TSUKAMURA, Hiroko |
author_sort | HORIHATA, Kei |
collection | PubMed |
description | Kisspeptin, encoded by Kiss1, is essential for reproduction in mammals. Kiss1 expression is regulated by estrogen via histone acetylation in the Kiss1 promotor region. Thus, elucidation of histone modification factor(s) involved in the regulation of Kiss1 expression is required to gain further understanding of the mechanisms of its control. The RNA-seq analysis of isolated kisspeptin neurons, obtained from the arcuate nucleus (ARC) of female rats, revealed that Rbbp7, encoding retinoblastoma binding protein 7 (RBBP7), a member of histone modification and chromatin remodeling complexes, is highly expressed in the ARC kisspeptin neurons. Thus, the present study aimed to investigate whether RBBP7 is involved in Kiss1 expression. Histological analysis using in situ hybridization (ISH) revealed that Rbbp7 expression was located in several hypothalamic nuclei, including the ARC and the anteroventral periventricular nucleus (AVPV), where kisspeptin neurons are located. Double ISH for Rbbp7 and Kiss1 showed that a majority of kisspeptin neurons (more than 85%) expressed Rbbp7 mRNA in both the ARC and the AVPV of female rats. Further, Rbbp7 mRNA knockdown significantly decreased in vitro expression of Kiss1 in a mouse immortalized kisspeptin neuronal cell line (mHypoA-55). Estrogen treatment significantly decreased and increased Kiss1 mRNA levels in the ARC and AVPV of ovariectomized female rats, respectively, but failed to affect Rbbp7 mRNA levels in both the nuclei. Taken together, these findings suggest that RBBP7 is involved in the upregulation of Kiss1 expression in kisspeptin neurons of rodents in an estrogen-independent manner. |
format | Online Article Text |
id | pubmed-7175387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Society for Reproduction and Development |
record_format | MEDLINE/PubMed |
spelling | pubmed-71753872020-04-27 Retinoblastoma binding protein 7 is involved in Kiss1 mRNA upregulation in rodents HORIHATA, Kei INOUE, Naoko UENOYAMA, Yoshihisa MAEDA, Kei-ichiro TSUKAMURA, Hiroko J Reprod Dev Original Article Kisspeptin, encoded by Kiss1, is essential for reproduction in mammals. Kiss1 expression is regulated by estrogen via histone acetylation in the Kiss1 promotor region. Thus, elucidation of histone modification factor(s) involved in the regulation of Kiss1 expression is required to gain further understanding of the mechanisms of its control. The RNA-seq analysis of isolated kisspeptin neurons, obtained from the arcuate nucleus (ARC) of female rats, revealed that Rbbp7, encoding retinoblastoma binding protein 7 (RBBP7), a member of histone modification and chromatin remodeling complexes, is highly expressed in the ARC kisspeptin neurons. Thus, the present study aimed to investigate whether RBBP7 is involved in Kiss1 expression. Histological analysis using in situ hybridization (ISH) revealed that Rbbp7 expression was located in several hypothalamic nuclei, including the ARC and the anteroventral periventricular nucleus (AVPV), where kisspeptin neurons are located. Double ISH for Rbbp7 and Kiss1 showed that a majority of kisspeptin neurons (more than 85%) expressed Rbbp7 mRNA in both the ARC and the AVPV of female rats. Further, Rbbp7 mRNA knockdown significantly decreased in vitro expression of Kiss1 in a mouse immortalized kisspeptin neuronal cell line (mHypoA-55). Estrogen treatment significantly decreased and increased Kiss1 mRNA levels in the ARC and AVPV of ovariectomized female rats, respectively, but failed to affect Rbbp7 mRNA levels in both the nuclei. Taken together, these findings suggest that RBBP7 is involved in the upregulation of Kiss1 expression in kisspeptin neurons of rodents in an estrogen-independent manner. The Society for Reproduction and Development 2020-01-19 2020-04 /pmc/articles/PMC7175387/ /pubmed/31956172 http://dx.doi.org/10.1262/jrd.2019-149 Text en ©2020 Society for Reproduction and Development This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Article HORIHATA, Kei INOUE, Naoko UENOYAMA, Yoshihisa MAEDA, Kei-ichiro TSUKAMURA, Hiroko Retinoblastoma binding protein 7 is involved in Kiss1 mRNA upregulation in rodents |
title | Retinoblastoma binding protein 7 is involved in Kiss1 mRNA upregulation in rodents |
title_full | Retinoblastoma binding protein 7 is involved in Kiss1 mRNA upregulation in rodents |
title_fullStr | Retinoblastoma binding protein 7 is involved in Kiss1 mRNA upregulation in rodents |
title_full_unstemmed | Retinoblastoma binding protein 7 is involved in Kiss1 mRNA upregulation in rodents |
title_short | Retinoblastoma binding protein 7 is involved in Kiss1 mRNA upregulation in rodents |
title_sort | retinoblastoma binding protein 7 is involved in kiss1 mrna upregulation in rodents |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7175387/ https://www.ncbi.nlm.nih.gov/pubmed/31956172 http://dx.doi.org/10.1262/jrd.2019-149 |
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