Literature DB >> 22980088

Expression patterns of sirtuin genes in porcine preimplantation embryos and effects of sirtuin inhibitors on in vitro embryonic development after parthenogenetic activation and in vitro fertilization.

Seong-Sung Kwak1, Seung-A Cheong, Junchul David Yoon, Yubyeol Jeon, Sang-Hwan Hyun.   

Abstract

We examined the expression patterns of porcine sirtuin 1 to 3 (Sirt1-3) genes in preimplantation embryos derived from parthenogenetic activation (PA), in vitro fertilization (IVF) and somatic cell nuclear transfer (SCNT). We also investigated the effects of sirtuin inhibitors (5 mM nicotinamide [NAM] and 100 μM sirtinol) on embryonic development of PA and IVF embryos under in vitro culture (IVC). The expression patterns of Sirt1-3 mRNA in preimplantation embryos of PA, IVF, and SCNT were significantly (P < 0.05) decreased from metaphase stage of oocyte to blastocyst stage. Especially, the expressions of Sirt1-3 in SCNT blastocysts were significantly (P < 0.05) lower and Sirt2 in PA blastocyst was significantly higher compared with the IVF blastocysts. Treatment with sirtuin inhibitors during IVC resulted in significantly (P < 0.05) decreased blastocyst formation and total cell number of blastocyst derived from PA (NAM: 29.4% and 29.6, sirtinol: 31.0% and 30.3, and control: 40.9% and 41.7, respectively) and IVF embryos (NAM: 10.4% and 30.9, sirtinol: 6.3% and 30.5, and control: 16.7% and 42.8, respectively). There was no significant difference in cleavage rate in both PA and IVF embryos. The early and expanded blastocyst formations at Day 7 were significantly lower in the sirtuin inhibitors-treated groups than the control. It was demonstrated that sirtuin inhibitor (NAM) influenced the percentage of blastocyst formation and total cell number of PA derived blastocyst when NAM was added during day 4 to 7 (22.1% and 32.4) or day 0 to 7 (23.1% and 31.6) of IVC compared with the control (41.8% and 41.5). No significant difference in cleavage rates appeared among the groups. The blastocysts derived from PA embryos treated with sirtuin inhibitors showed lower (P < 0.05) expressions of POU5F1 and Cdx2 genes. Also, Sirt2 mRNA expression was significantly decreased in sirtinol treated group and Sirt3 mRNA expression was also significantly decreased in both NAM and sirtinol treated groups compared with the control. In conclusion, these results suggest that sirtuins may have a physiological and important role in embryonic development of porcine preimplantation embryos by regulating essential gene expressions of developing embryos. These findings could have implications for understanding the role of sirtuins during embryo development and for improving SCNT and related techniques.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22980088     DOI: 10.1016/j.theriogenology.2012.07.006

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  15 in total

1.  Sirt2 functions in spindle organization and chromosome alignment in mouse oocyte meiosis.

Authors:  Liang Zhang; Xiaojing Hou; Rujun Ma; Kelle Moley; Tim Schedl; Qiang Wang
Journal:  FASEB J       Date:  2013-12-12       Impact factor: 5.191

2.  Transcriptome Analysis of Pig In Vivo, In Vitro-Fertilized, and Nuclear Transfer Blastocyst-Stage Embryos Treated with Histone Deacetylase Inhibitors Postfusion and Activation Reveals Changes in the Lysosomal Pathway.

Authors:  Kristin M Whitworth; Jiude Mao; Kiho Lee; William G Spollen; Melissa S Samuel; Eric M Walters; Lee D Spate; Randall S Prather
Journal:  Cell Reprogram       Date:  2015-08       Impact factor: 1.987

3.  Sirtuin Inhibition Adversely Affects Porcine Oocyte Meiosis.

Authors:  Liang Zhang; Rujun Ma; Jin Hu; Xiaolin Ding; Yinxue Xu
Journal:  PLoS One       Date:  2015-07-15       Impact factor: 3.240

Review 4.  Sirtuin Functions in Female Fertility: Possible Role in Oxidative Stress and Aging.

Authors:  Carla Tatone; Giovanna Di Emidio; Maurizio Vitti; Michela Di Carlo; Silvano Santini; Anna Maria D'Alessandro; Stefano Falone; Fernanda Amicarelli
Journal:  Oxid Med Cell Longev       Date:  2015-05-05       Impact factor: 6.543

5.  Modification of mitochondrial function, cytoplasmic lipid content and cryosensitivity of bovine embryos by resveratrol.

Authors:  Takahito Abe; Ryouka Kawahara-Miki; Tomotaka Hara; Tatsuo Noguchi; Takeshi Hayashi; Koumei Shirasuna; Takehito Kuwayama; Hisataka Iwata
Journal:  J Reprod Dev       Date:  2017-06-09       Impact factor: 2.214

6.  Nicotinamide Supplementation during the In Vitro Maturation of Oocytes Improves the Developmental Competence of Preimplantation Embryos: Potential Link to SIRT1/AKT Signaling.

Authors:  Marwa El Sheikh; Ahmed Atef Mesalam; Muhammad Idrees; Tabinda Sidrat; Ayman Mesalam; Kyeong-Lim Lee; Il-Keun Kong
Journal:  Cells       Date:  2020-06-25       Impact factor: 6.600

7.  Epigenetic and non-epigenetic mode of SIRT1 action during oocyte meiosis progression.

Authors:  Jan Nevoral; Lukas Landsmann; Miriam Stiavnicka; Petr Hosek; Jiri Moravec; Sarka Prokesova; Hedvika Rimnacova; Eliska Koutna; Pavel Klein; Kristyna Hoskova; Tereza Zalmanova; Tereza Fenclova; Jaroslav Petr; Milena Kralickova
Journal:  J Anim Sci Biotechnol       Date:  2019-08-09

8.  Melatonin Alleviates the Toxicity of High Nicotinamide Concentrations in Oocytes: Potential Interaction with Nicotinamide Methylation Signaling.

Authors:  Marwa El-Sheikh; Ahmed Atef Mesalam; Seok-Hwan Song; Jonghyeok Ko; Il-Keun Kong
Journal:  Oxid Med Cell Longev       Date:  2021-04-08       Impact factor: 6.543

9.  SIRT1, 2, 3 protect mouse oocytes from postovulatory aging.

Authors:  Teng Zhang; Yang Zhou; Li Li; Hong-Hui Wang; Xue-Shan Ma; Wei-Ping Qian; Wei Shen; Heide Schatten; Qing-Yuan Sun
Journal:  Aging (Albany NY)       Date:  2016-04       Impact factor: 5.682

10.  SIRT1-dependent modulation of methylation and acetylation of histone H3 on lysine 9 (H3K9) in the zygotic pronuclei improves porcine embryo development.

Authors:  Katerina Adamkova; Young-Joo Yi; Jaroslav Petr; Tereza Zalmanova; Kristyna Hoskova; Pavla Jelinkova; Jiri Moravec; Milena Kralickova; Miriam Sutovsky; Peter Sutovsky; Jan Nevoral
Journal:  J Anim Sci Biotechnol       Date:  2017-11-01
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