Literature DB >> 20619978

Expression analysis of circadian genes in oocytes and preimplantation embryos of cattle and rabbits.

Tomoko Amano1, Kaori Tokunaga, Reiko Kakegawa, Ayaka Yanagisawa, Atsushi Takemoto, Atsuhiro Tatemizo, Tatsuya Watanabe, Yuki Hatanaka, Akinori Matsushita, Masao Kishi, Masayuki Anzai, Hiromi Kato, Tasuku Mitani, Satoshi Kishigami, Kazuhiro Saeki, Yoshihiko Hosoi, Akira Iritani, Kazuya Matsumoto.   

Abstract

We previously showed that circadian genes clock, bmal1, cry1, cry2, per1, and per2 are expressed and function as maternal mRNA regulating events in the oocytes and preimplantation embryos of mice. Recent evidence indicates however that either or both expression profiles of circadian genes in some tissues, and transcript sequences of circadian genes, differ to generate the physiological differences between diurnal and nocturnal species. We therefore investigated the expression profiles of circadian genes in oocytes and preimplantation embryos of species other than mice, namely cattle and rabbits, representing diurnal and nocturnal species, respectively, and determined the protein sequences of circadian genes in these species. Quantitative real-time PCR revealed that all circadian genes considered in this study were present in the oocytes and preimplantation embryos of both species, and the transcript amounts of clock, cry1 and per1 contained in oocytes were significantly higher than in preimplantation embryos of both species. The transcripts of clock, cry1, and per1 of cattle and rabbits were determined by primer walking, and functional domains in the estimated amino acid sequences were compared between cattle and rabbits and with those of humans and mice. The sequences of clock, cry1, and per1 in cattle and rabbits closely resembled those in mice (85-100% homologies), and no difference based on diurnality or nocturnality was observed. These findings suggest that circadian genes in the oocytes and preimplantation embryos of mammals fulfill the same functions across species as maternal mRNA. 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20619978     DOI: 10.1016/j.anireprosci.2010.05.020

Source DB:  PubMed          Journal:  Anim Reprod Sci        ISSN: 0378-4320            Impact factor:   2.145


  6 in total

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Journal:  Int J Mol Sci       Date:  2017-06-14       Impact factor: 5.923

Review 2.  The Circadian Physiology: Implications in Livestock Health.

Authors:  Hao Li; Kaiqi Li; Kexin Zhang; Yanwei Li; Haotian Gu; Haoyu Liu; Zhangping Yang; Demin Cai
Journal:  Int J Mol Sci       Date:  2021-02-20       Impact factor: 5.923

Review 3.  Circadian Rhythms Within the Female HPG Axis: From Physiology to Etiology.

Authors:  Shuyi Shao; Huanqiang Zhao; Zhiying Lu; Xiaohong Lei; Ying Zhang
Journal:  Endocrinology       Date:  2021-08-01       Impact factor: 4.736

4.  Functional analysis of nocturnin, a circadian deadenylase, at maternal-to-zygotic transition in mice.

Authors:  Satoshi Nishikawa; Yuki Hatanaka; Mikiko Tokoro; Seung-Wook Shin; Natsumi Shimizu; Takuji Nishihara; Rie Kato; Atsushi Takemoto; Tomoko Amano; Masayuki Anzai; Satoshi Kishigami; Yoshihiko Hosoi; Kazuya Matsumoto
Journal:  J Reprod Dev       Date:  2013-03-01       Impact factor: 2.214

5.  Domestication may affect the maternal mRNA profile in unfertilized eggs, potentially impacting the embryonic development of Eurasian perch (Perca fluviatilis).

Authors:  Tainá Rocha de Almeida; Maud Alix; Aurélie Le Cam; Christophe Klopp; Jérôme Montfort; Lola Toomey; Yannick Ledoré; Julien Bobe; Dominique Chardard; Bérénice Schaerlinger; Pascal Fontaine
Journal:  PLoS One       Date:  2019-12-31       Impact factor: 3.240

6.  Fine mapping of genomic regions associated with female fertility in Nellore beef cattle based on sequence variants from segregating sires.

Authors:  Gerson A Oliveira Júnior; Daniel J A Santos; Aline S M Cesar; Solomon A Boison; Ricardo V Ventura; Bruno C Perez; José F Garcia; José Bento S Ferraz; Dorian J Garrick
Journal:  J Anim Sci Biotechnol       Date:  2019-12-16
  6 in total

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