Suppr超能文献

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.

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。

相似文献

3
Mcrs1 interacts with Six1 to influence early craniofacial and otic development.
Dev Biol. 2020 Nov 1;467(1-2):39-50. doi: 10.1016/j.ydbio.2020.08.013. Epub 2020 Sep 3.
6
Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development.
Dev Biol. 2017 Jan 15;421(2):171-182. doi: 10.1016/j.ydbio.2016.11.021. Epub 2016 Dec 9.
7
Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation.
Dev Biol. 2019 Feb 1;446(1):68-79. doi: 10.1016/j.ydbio.2018.12.003. Epub 2018 Dec 6.
8
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes.
J Exp Zool B Mol Dev Evol. 2024 May;342(3):212-240. doi: 10.1002/jez.b.23222. Epub 2023 Oct 13.
10
Targets of the transcription factor Six1 identify previously unreported candidate deafness genes.
Development. 2025 Apr 1;152(7). doi: 10.1242/dev.204533. Epub 2025 Apr 11.

引用本文的文献

1
Proliferation associated 2G4 is required for the ciliation of vertebrate motile cilia.
Commun Biol. 2024 Nov 4;7(1):1430. doi: 10.1038/s42003-024-07150-0.
2
Bop1 is required to establish precursor domains of craniofacial tissues.
Genesis. 2024 Feb;62(1):e23580. doi: 10.1002/dvg.23580. Epub 2023 Nov 16.
3
Zmym4 is required for early cranial gene expression and craniofacial cartilage formation.
Front Cell Dev Biol. 2023 Oct 3;11:1274788. doi: 10.3389/fcell.2023.1274788. eCollection 2023.
4
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes.
J Exp Zool B Mol Dev Evol. 2024 May;342(3):212-240. doi: 10.1002/jez.b.23222. Epub 2023 Oct 13.
5
The sulfotransferase XB5850668.L is required to apportion embryonic ectodermal domains.
Dev Dyn. 2023 Dec;252(12):1407-1427. doi: 10.1002/dvdy.648. Epub 2023 Aug 19.
6
Functions of block of proliferation 1 during anterior development in Xenopus laevis.
PLoS One. 2022 Aug 25;17(8):e0273507. doi: 10.1371/journal.pone.0273507. eCollection 2022.
7
Mcrs1 is required for branchial arch and cranial cartilage development.
Dev Biol. 2022 Sep;489:62-75. doi: 10.1016/j.ydbio.2022.06.002. Epub 2022 Jun 11.
8
Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease.
Genesis. 2021 Dec;59(12):e23453. doi: 10.1002/dvg.23453. Epub 2021 Oct 19.

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.
Dev Biol. 2010 Aug 1;344(1):158-71. doi: 10.1016/j.ydbio.2010.04.029. Epub 2010 May 21.
3
Activation of Six1 target genes is required for sensory placode formation.
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.
Dev Biol. 2009 Oct 15;334(2):409-17. doi: 10.1016/j.ydbio.2009.07.039. Epub 2009 Aug 3.
7
Deficiency in Six2 during prenatal development is associated with reduced nephron number, chronic renal failure, and hypertension in Br/+ adult mice.
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.
Science. 2009 Feb 20;323(5917):1074-7. doi: 10.1126/science.1166859. Epub 2009 Jan 1.
9
Pleiotropic effects in Eya3 knockout mice.
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.
BMC Cell Biol. 2008 Dec 18;9:69. doi: 10.1186/1471-2121-9-69.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验