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启动减数分裂:视黄酸的案例。

Initiating meiosis: the case for retinoic acid.

机构信息

School of Molecular Biosciences, Washington State University, Pullman, 99164, USA.

出版信息

Biol Reprod. 2012 Feb 14;86(2):35. doi: 10.1095/biolreprod.111.096610. Print 2012 Feb.

DOI:10.1095/biolreprod.111.096610
PMID:22075477
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3290665/
Abstract

The requirement for vitamin A in reproduction and development was first determined from studies of nutritional deficiencies. Subsequent research has shown that embryonic development and both male and female reproduction are modulated by retinoic acid (RA), the active form of vitamin A. Because RA is active in multiple developmental systems, its synthesis, transport, and degradation are tightly regulated in different tissues. A growing body of evidence implicates RA as a requirement for the initiation of meiosis in both male and female mammals, resulting in a mechanistic model involving the interplay of RA, RA synthesis enzymes, RA receptors, and degradative cytochrome P450 enzymes in this system. Recently, that model has been challenged, prompting a review of the established paradigm. While it remains possible that additional molecules may be involved in regulating entry into meiosis, the weight of evidence supporting a key role for RA is incontrovertible.

摘要

维生素 A 在生殖和发育中的需求最初是从营养缺乏研究中确定的。随后的研究表明,视黄酸(RA),即维生素 A 的活性形式,调节胚胎发育和雄性及雌性生殖。由于 RA 在多个发育系统中都具有活性,因此其合成、运输和降解在不同组织中受到严格调控。越来越多的证据表明,RA 是雄性和雌性哺乳动物减数分裂起始的必需物质,这导致了一个涉及 RA、RA 合成酶、RA 受体和该系统中降解细胞色素 P450 酶相互作用的机制模型。最近,该模型受到了挑战,促使人们对既定范式进行了审查。虽然仍有可能有其他分子参与调节进入减数分裂,但支持 RA 关键作用的证据是无可争议的。

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本文引用的文献

1
Retinoic Acid signalling and the control of meiotic entry in the human fetal gonad.维甲酸信号转导与人类胎儿性腺中减数分裂起始的调控。
PLoS One. 2011;6(6):e20249. doi: 10.1371/journal.pone.0020249. Epub 2011 Jun 3.
2
DMRT1 promotes oogenesis by transcriptional activation of Stra8 in the mammalian fetal ovary.DMRT1 通过转录激活哺乳动物胎儿卵巢中的 Stra8 来促进卵子发生。
Dev Biol. 2011 Aug 1;356(1):63-70. doi: 10.1016/j.ydbio.2011.05.658. Epub 2011 May 20.
3
Sex-specific timing of meiotic initiation is regulated by Cyp26b1 independent of retinoic acid signalling.减数分裂起始的性别特异性时间由Cyp26b1调控,且独立于视黄酸信号通路。
Nat Commun. 2011 Jan 11;2:151. doi: 10.1038/ncomms1136.
4
Suppression of Stra8 expression in the mouse gonad by WIN 18,446.WIN 18,446 抑制小鼠性腺中 Stra8 的表达。
Biol Reprod. 2011 May;84(5):957-65. doi: 10.1095/biolreprod.110.088575. Epub 2011 Jan 5.
5
The mammalian doublesex homolog DMRT1 is a transcriptional gatekeeper that controls the mitosis versus meiosis decision in male germ cells.哺乳动物双性基因同源物 DMRT1 是一个转录主控因子,控制着精母细胞向有丝分裂还是减数分裂的命运。
Dev Cell. 2010 Oct 19;19(4):612-24. doi: 10.1016/j.devcel.2010.09.010.
6
Vitamin A deficiency results in meiotic failure and accumulation of undifferentiated spermatogonia in prepubertal mouse testis.维生素 A 缺乏导致减数分裂失败和未分化精原细胞在青春期前小鼠睾丸中积累。
Biol Reprod. 2011 Feb;84(2):336-41. doi: 10.1095/biolreprod.110.086157. Epub 2010 Sep 29.
7
FGF9 suppresses meiosis and promotes male germ cell fate in mice.FGF9 抑制减数分裂并促进小鼠雄性生殖细胞的命运。
Dev Cell. 2010 Sep 14;19(3):440-9. doi: 10.1016/j.devcel.2010.08.010.
8
Direct effects of retinoic acid on entry of fetal male germ cells into meiosis in mice.视黄酸对小鼠雄性生殖细胞进入减数分裂的直接影响。
Biol Reprod. 2010 Dec;83(6):1056-63. doi: 10.1095/biolreprod.110.085787. Epub 2010 Sep 8.
9
New testicular mechanisms involved in the prevention of fetal meiotic initiation in mice.新的睾丸机制参与预防小鼠的胎儿减数分裂起始。
Dev Biol. 2010 Oct 15;346(2):320-30. doi: 10.1016/j.ydbio.2010.08.002. Epub 2010 Aug 11.
10
Suppression of spermatogenesis by bisdichloroacetyldiamines is mediated by inhibition of testicular retinoic acid biosynthesis.双二氯乙酰二胺对精子发生的抑制作用是通过抑制睾丸视黄酸生物合成介导的。
J Androl. 2011 Jan-Feb;32(1):111-9. doi: 10.2164/jandrol.110.010751. Epub 2010 Aug 12.