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本文引用的文献

1
Conserved expression of mouse Six1 in the pre-placodal region (PPR) and identification of an enhancer for the rostral PPR.鼠 Six1 在脑前嵴区域(PPR)中的保守表达及鉴定出一个用于 PPR 区域的增强子。
Dev Biol. 2010 Aug 1;344(1):158-71. doi: 10.1016/j.ydbio.2010.04.029. Epub 2010 May 21.
2
HAGE, a cancer/testis antigen expressed at the protein level in a variety of cancers.HAGE是一种在多种癌症中在蛋白质水平表达的癌/睾丸抗原。
Cancer Immun. 2010 Jan 11;10:2.
3
Activation of Six1 target genes is required for sensory placode formation.Six1靶基因的激活是感觉基板形成所必需的。
Dev Biol. 2009 Dec 15;336(2):327-36. doi: 10.1016/j.ydbio.2009.09.025. Epub 2009 Sep 23.
4
Six2 activity is required for the formation of the mammalian pyloric sphincter.Six2活性是哺乳动物幽门括约肌形成所必需的。
Dev Biol. 2009 Oct 15;334(2):409-17. doi: 10.1016/j.ydbio.2009.07.039. Epub 2009 Aug 3.
5
EYA4, deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts with SIX3 both physically and functionally.在一例半叶全前脑畸形中间型病例中缺失的EYA4,在物理和功能上均与SIX3相互作用。
Hum Mutat. 2009 Oct;30(10):E946-55. doi: 10.1002/humu.21094.
6
A systematic analysis of Tinman function reveals Eya and JAK-STAT signaling as essential regulators of muscle development.对Tinman功能的系统分析表明,Eya和JAK-STAT信号传导是肌肉发育的重要调节因子。
Dev Cell. 2009 Feb;16(2):280-91. doi: 10.1016/j.devcel.2009.01.006.
7
Deficiency in Six2 during prenatal development is associated with reduced nephron number, chronic renal failure, and hypertension in Br/+ adult mice.产前发育期间Six2的缺乏与Br/+成年小鼠的肾单位数量减少、慢性肾衰竭和高血压有关。
Am J Physiol Renal Physiol. 2009 May;296(5):F1166-78. doi: 10.1152/ajprenal.90550.2008. Epub 2009 Feb 4.
8
Neuronal activity-induced Gadd45b promotes epigenetic DNA demethylation and adult neurogenesis.神经元活动诱导的Gadd45b促进表观遗传DNA去甲基化和成年神经发生。
Science. 2009 Feb 20;323(5917):1074-7. doi: 10.1126/science.1166859. Epub 2009 Jan 1.
9
Pleiotropic effects in Eya3 knockout mice.Eya3基因敲除小鼠中的多效性效应。
BMC Dev Biol. 2008 Dec 22;8:118. doi: 10.1186/1471-213X-8-118.
10
Alterations in cell growth and signaling in ErbB3 binding protein-1 (Ebp1) deficient mice.ErbB3结合蛋白-1(Ebp1)缺陷小鼠的细胞生长和信号传导改变。
BMC Cell Biol. 2008 Dec 18;9:69. doi: 10.1186/1471-2121-9-69.

脊椎动物六类转录因子候选共因子的发育表达模式。

Developmental expression patterns of candidate cofactors for vertebrate six family transcription factors.

机构信息

Department of Anatomy and Regenerative Biology, The George Washington University, School of Medicine and Health Sciences, Washington, DC 20037, USA.

出版信息

Dev Dyn. 2010 Dec;239(12):3446-66. doi: 10.1002/dvdy.22484.

DOI:10.1002/dvdy.22484
PMID:21089078
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3059517/
Abstract

Six family transcription factors play important roles in craniofacial development. Their transcriptional activity can be modified by cofactor proteins. Two Six genes and one cofactor gene (Eya1) are involved in the human Branchio-otic (BO) and Branchio-otic-renal (BOR) syndromes. However, mutations in Six and Eya genes only account for approximately half of these patients. To discover potential new causative genes, we searched the Xenopus genome for orthologues of Drosophila cofactor proteins that interact with the fly Six-related factor, SO. We identified 33 Xenopus genes with high sequence identity to 20 of the 25 fly SO-interacting proteins. We provide the developmental expression patterns of the Xenopus orthologues for 11 of the fly genes, and demonstrate that all are expressed in developing craniofacial tissues with at least partial overlap with Six1/Six2. We speculate that these genes may function as Six-interacting partners with important roles in vertebrate craniofacial development and perhaps congenital syndromes.

摘要

六个家族转录因子在颅面发育中发挥重要作用。它们的转录活性可以通过辅助因子蛋白来修饰。两个 Six 基因和一个辅助因子基因(Eya1)参与了人类的 Branchio-otic(BO)和 Branchio-otic-renal(BOR)综合征。然而,Six 和 Eya 基因突变仅占这些患者的大约一半。为了发现潜在的新的致病基因,我们在 Xenopus 基因组中搜索与果蝇 Six 相关因子相互作用的果蝇辅助因子蛋白的同源物。我们鉴定了 33 个与 25 个果蝇 SO 相互作用蛋白中的 20 个具有高度序列同一性的 Xenopus 基因。我们提供了 11 个果蝇基因的 Xenopus 同源物的发育表达模式,并证明它们都在发育中的颅面组织中表达,与 Six1/Six2 至少有部分重叠。我们推测这些基因可能作为 Six 的相互作用伙伴,在脊椎动物颅面发育和可能的先天性综合征中发挥重要作用。