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      Pivotal role of High-Mobility Group Box 2 in ovarian folliculogenesis and fertility

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          Abstract

          Background

          High-Mobility Group Box 1 (HMGB1) and HMGB2 are chromatin-associated proteins that belong to the HMG protein family, and are involved in the regulation of DNA transcription during cell differentiation, proliferation and regeneration in various tissues. However, the role of HMGB2 in ovarian folliculogenesis is largely unknown.

          Methods

          We investigated the functional role of HMGB1 and HMGB2 in ovarian folliculogenesis and fertilization using C57BL/6 wild type (WT) and HMGB2-knockout (KO) mice. Ovarian tissues were obtained from WT and HMGB2-KO mice at postnatal days 0, 3, 7, and 2, 6 months of age, then performed immunohistochemistry, qPCR and Western blotting analyses. Oocyte fertilization capability was examined by natural breeding and in vitro fertilization experiments.

          Results

          In HMGB2-KO mice, ovary weight was decreased due to reduced numbers of oocytes and follicles. Natural breeding and in vitro fertilization results indicated that HMGB2-KO mice are subfertile, but not sterile. Immunohistochemistry showed that oocytes expressed HMGB2, but not HMGB1, in neonatal and adult WT ovaries. Interestingly, in HMGB2-KO ovaries, a compensatory increase in HMGB1 was found in oocyte nuclei of neonatal and 2-month-old mice; however, this was lost at 6 months of age.

          Conclusions

          The depletion of HMGB2 led to alterations in ovarian morphology and function, suggesting that HMGB2 plays an essential role in ovarian development, folliculogenesis and fertilization.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s13048-022-01071-4.

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          Most cited references32

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          HMG proteins: dynamic players in gene regulation and differentiation.

          Core histones package the genome into nucleosomes and control its accessibility to transcription factors. High mobility group proteins (HMGs) are, after histones, the second most abundant chromatin proteins and exert global genomic functions in establishing active or inactive chromatin domains. It is becoming increasingly clear that they also specifically control the expression of a limited number of genes. Moreover, they contribute to the fine tuning of transcription in response to rapid environmental changes. They do so by interacting with nucleosomes, transcription factors, nucleosome-remodelling machines, and with histone H1.
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            Intraovarian Control of Early Folliculogenesis

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              HMGB2 Loss upon Senescence Entry Disrupts Genomic Organization and Induces CTCF Clustering across Cell Types.

              Processes like cellular senescence are characterized by complex events giving rise to heterogeneous cell populations. However, the early molecular events driving this cascade remain elusive. We hypothesized that senescence entry is triggered by an early disruption of the cells' three-dimensional (3D) genome organization. To test this, we combined Hi-C, single-cell and population transcriptomics, imaging, and in silico modeling of three distinct cells types entering senescence. Genes involved in DNA conformation maintenance are suppressed upon senescence entry across all cell types. We show that nuclear depletion of the abundant HMGB2 protein occurs early on the path to senescence and coincides with the dramatic spatial clustering of CTCF. Knocking down HMGB2 suffices for senescence-induced CTCF clustering and for loop reshuffling, while ectopically expressing HMGB2 rescues these effects. Our data suggest that HMGB2-mediated genomic reorganization constitutes a primer for the ensuing senescent program.
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                Author and article information

                Contributors
                narantsog@med.miyazaki-u.ac.jp
                Journal
                J Ovarian Res
                J Ovarian Res
                Journal of Ovarian Research
                BioMed Central (London )
                1757-2215
                20 December 2022
                20 December 2022
                2022
                : 15
                : 133
                Affiliations
                [1 ]GRID grid.410849.0, ISNI 0000 0001 0657 3887, Department of Anatomy, Histochemistry and Cell Biology, Faculty of Medicine, , University of Miyazaki, ; 5200, 889-1692 Kihara, Kiyotake, Miyazaki Japan
                [2 ]GRID grid.410849.0, ISNI 0000 0001 0657 3887, Department of Oral and Maxillofacial Surgery, Faculty of Medicine, , University of Miyazaki, ; 5200, 889-1692 Kihara, Kiyotake, Miyazaki Japan
                [3 ]GRID grid.410849.0, ISNI 0000 0001 0657 3887, Department of Ophthalmology, Faculty of Medicine, , University of Miyazaki, ; 5200, 889-1692 Kihara, Kiyotake, Miyazaki Japan
                [4 ]GRID grid.410849.0, ISNI 0000 0001 0657 3887, Division of Bio-resources, Department of Biotechnology, Frontier Science Research Center, , University of Miyazaki, ; Kihara, Kiyotake, Miyazaki 5200, 889-1692 Japan
                [5 ]GRID grid.410849.0, ISNI 0000 0001 0657 3887, Department of Surgery, Faculty of Medicine, , University of Miyazaki, ; Kihara, Kiyotake, Miyazaki, 889–1692 Japan
                [6 ]GRID grid.410849.0, ISNI 0000 0001 0657 3887, Department of Orthopaedic Surgery, Faculty of Medicine, , University of Miyazaki, ; 5200, 889-1692 Kihara, Kiyotake, Miyazaki Japan
                Article
                1071
                10.1186/s13048-022-01071-4
                9769043
                36539852
                3a1ec58e-3a58-4087-90bc-28f7afc44c54
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 13 October 2022
                : 8 December 2022
                Funding
                Funded by: Grant for Clinical Research from Miyazaki University Hospital
                Funded by: FundRef http://dx.doi.org/10.13039/501100001691, Japan Society for the Promotion of Science;
                Award ID: 19K16477
                Award ID: 16K08471, 21K06738
                Categories
                Research
                Custom metadata
                © The Author(s) 2022

                Obstetrics & Gynecology
                hmgb2,ovary,folliculogenesis,fertility,hmgb1
                Obstetrics & Gynecology
                hmgb2, ovary, folliculogenesis, fertility, hmgb1

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