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本文引用的文献

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Heterozygous deletion of ventral anterior homeobox (vax1) causes subfertility in mice.腹侧前同源盒基因1(vax1)杂合缺失导致小鼠生育力低下。
Endocrinology. 2014 Oct;155(10):4043-53. doi: 10.1210/en.2014-1277. Epub 2014 Jul 25.
2
Forkhead box O1 is a repressor of basal and GnRH-induced Fshb transcription in gonadotropes.叉头框蛋白O1是促性腺激素细胞中基础及促性腺激素释放激素诱导的促卵泡激素β亚基转录的抑制因子。
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Efficient, specific, developmentally appropriate cre-mediated recombination in anterior pituitary gonadotropes and thyrotropes.在垂体前叶促性腺细胞和促甲状腺细胞中实现高效、特异性且发育阶段适宜的cre介导的重组。
Genesis. 2013 Nov;51(11):785-92. doi: 10.1002/dvg.22425. Epub 2013 Sep 2.
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Aberrant development of the suprachiasmatic nucleus and circadian rhythms in mice lacking the homeodomain protein Six6.缺失同源域蛋白 Six6 的小鼠中视交叉上核和昼夜节律的异常发育。
J Biol Rhythms. 2013 Feb;28(1):15-25. doi: 10.1177/0748730412468084.
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Msx1 homeodomain protein represses the αGSU and GnRH receptor genes during gonadotrope development.Msx1同源结构域蛋白在促性腺激素细胞发育过程中抑制α亚基糖蛋白激素和促性腺激素释放激素受体基因。
Mol Endocrinol. 2013 Mar;27(3):422-36. doi: 10.1210/me.2012-1289. Epub 2013 Jan 31.
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Hypothalamic dysregulation and infertility in mice lacking the homeodomain protein Six6.Six6 同源域蛋白缺失的小鼠下丘脑失调和不孕。
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7
LIM homeodomain transcription factor Isl-1 enhances follicle stimulating hormone-beta and luteinizing hormone-beta gene expression and mediates the activation of leptin on gonadotropin synthesis.LIM 同源框转录因子 Isl-1 增强促卵泡激素-β 和促黄体生成素-β 基因的表达,并介导瘦素对促性腺激素合成的激活。
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Corepressors TLE1 and TLE3 interact with HESX1 and PROP1.共抑制因子TLE1和TLE3与HESX1和PROP1相互作用。
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10
NeuroD1 and Mash1 temporally regulate GnRH receptor gene expression in immortalized mouse gonadotrope cells.神经分化因子1(NeuroD1)和achaete-scute同源物1(Mash1)在永生化小鼠促性腺激素细胞中对促性腺激素释放激素(GnRH)受体基因表达进行时间调控。
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同源域蛋白SIX3和SIX6在垂体发育过程中调节促性腺激素细胞特异性基因。

Homeodomain Proteins SIX3 and SIX6 Regulate Gonadotrope-specific Genes During Pituitary Development.

作者信息

Xie Huimin, Hoffmann Hanne M, Meadows Jason D, Mayo Susan L, Trang Crystal, Leming Sunamita S, Maruggi Chiara, Davis Shannon W, Larder Rachel, Mellon Pamela L

机构信息

Department of Reproductive Medicine and the Center for Reproductive Science and Medicine (H.X., H.M.H., J.D.M., S.L.M., C.T., S.S.L., C.M., R.L., P.L.M.), University of California, San Diego, La Jolla, California 92093; and Department of Human Genetics (S.W.D.), University of Michigan, Ann Arbor, Michigan 48109.

出版信息

Mol Endocrinol. 2015 Jun;29(6):842-55. doi: 10.1210/me.2014-1279. Epub 2015 Apr 27.

DOI:10.1210/me.2014-1279
PMID:25915183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4447639/
Abstract

Sine oculis-related homeobox 3 (SIX3) and SIX6, 2 closely related homeodomain transcription factors, are involved in development of the mammalian neuroendocrine system and mutations of Six6 adversely affect fertility in mice. We show that both small interfering RNA knockdown in gonadotrope cell lines and knockout of Six6 in both embryonic and adult male mice (Six6 knockout) support roles for SIX3 and SIX6 in transcriptional regulation in gonadotrope gene expression and that SIX3 and SIX6 can functionally compensate for each other. Six3 and Six6 expression patterns in gonadotrope cell lines reflect the timing of the expression of pituitary markers they regulate. Six3 is expressed in an immature gonadotrope cell line and represses transcription of the early lineage-specific pituitary genes, GnRH receptor (GnRHR) and the common α-subunit (Cga), whereas Six6 is expressed in a mature gonadotrope cell line and represses the specific β-subunits of LH and FSH (LHb and FSHb) that are expressed later in development. We show that SIX6 repression requires interaction with transducin-like enhancer of split corepressor proteins and competition for DNA-binding sites with the transcriptional activator pituitary homeobox 1. Our studies also suggest that estradiol and circadian rhythm regulate pituitary expression of Six6 and Six3 in adult females but not in males. In summary, SIX3 and SIX6 play distinct but compensatory roles in regulating transcription of gonadotrope-specific genes as gonadotrope cells differentiate.

摘要

正弦眼相关同源框3(SIX3)和SIX6是两个密切相关的同源结构域转录因子,参与哺乳动物神经内分泌系统的发育,Six6的突变会对小鼠的生育能力产生不利影响。我们发现,在促性腺激素细胞系中进行小干扰RNA敲低以及在胚胎期和成年雄性小鼠中敲除Six6(Six6基因敲除)均表明,SIX3和SIX6在促性腺激素基因表达的转录调控中发挥作用,并且SIX3和SIX6在功能上可以相互补偿。促性腺激素细胞系中Six3和Six6的表达模式反映了它们所调控的垂体标志物表达的时间。Six3在未成熟的促性腺激素细胞系中表达,并抑制早期谱系特异性垂体基因促性腺激素释放激素受体(GnRHR)和共同α亚基(Cga)的转录,而Six6在成熟的促性腺激素细胞系中表达,并抑制在发育后期表达的促黄体生成素和促卵泡生成素的特异性β亚基(LHβ和FSHβ)。我们发现,SIX6的抑制需要与分裂抑制蛋白转导素样增强子相互作用,并与转录激活因子垂体同源框1竞争DNA结合位点。我们的研究还表明,雌二醇和昼夜节律调节成年雌性而非雄性垂体中Six6和Six3的表达。总之,在促性腺激素细胞分化过程中,SIX3和SIX6在调节促性腺激素特异性基因的转录中发挥着不同但互补的作用。