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本文引用的文献

1
An atypical canonical bone morphogenetic protein (BMP) signaling pathway regulates Msh homeobox 1 (Msx1) expression during odontogenesis.非典型经典的骨形态发生蛋白(BMP)信号通路在牙发生过程中调节同源盒基因 1(Msx1)的表达。
J Biol Chem. 2014 Nov 7;289(45):31492-502. doi: 10.1074/jbc.M114.600064. Epub 2014 Oct 1.
2
Sox2 cooperates with inflammation-mediated Stat3 activation in the malignant transformation of foregut basal progenitor cells.Sox2 与炎症介导的 Stat3 激活在前肠基底祖细胞的恶性转化中协同作用。
Cell Stem Cell. 2013 Mar 7;12(3):304-15. doi: 10.1016/j.stem.2013.01.007.
3
Sox2 marks epithelial competence to generate teeth in mammals and reptiles.Sox2 标记哺乳动物和爬行动物中产生牙齿的上皮细胞的能力。
Development. 2013 Apr;140(7):1424-32. doi: 10.1242/dev.089599. Epub 2013 Mar 5.
4
Hedgehog-Gli activators direct osteo-chondrogenic function of bone morphogenetic protein toward osteogenesis in the perichondrium. hedgehog-Gli 激活物将骨形态发生蛋白的骨-软骨生成功能定向为软骨膜成骨。
J Biol Chem. 2013 Apr 5;288(14):9924-9932. doi: 10.1074/jbc.M112.409342. Epub 2013 Feb 19.
5
Cytoplasmic plaque formation in hemidesmosome development is dependent on SoxF transcription factor function.细胞质斑在半桥粒发育中的形成依赖于 SoxF 转录因子的功能。
PLoS One. 2012;7(9):e43857. doi: 10.1371/journal.pone.0043857. Epub 2012 Sep 4.
6
Expression pattern of Sox2 during mouse tooth development.Sox2在小鼠牙齿发育过程中的表达模式。
Gene Expr Patterns. 2012 Aug-Sep;12(7-8):273-81. doi: 10.1016/j.gep.2012.07.001. Epub 2012 Jul 24.
7
Sox2+ stem cells contribute to all epithelial lineages of the tooth via Sfrp5+ progenitors.Sox2+ 干细胞通过 Sfrp5+ 祖细胞为牙齿的所有上皮谱系做出贡献。
Dev Cell. 2012 Aug 14;23(2):317-28. doi: 10.1016/j.devcel.2012.05.012. Epub 2012 Jul 19.
8
WT1 and Sox11 regulate synergistically the promoter of the Wnt4 gene that encodes a critical signal for nephrogenesis.WT1 和 Sox11 协同调节编码肾发生关键信号的 Wnt4 基因的启动子。
Exp Cell Res. 2012 Jun 10;318(10):1134-45. doi: 10.1016/j.yexcr.2012.03.008. Epub 2012 Mar 17.
9
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.SOX5 基因在 12p12.1 上的杂合性缺失与发育迟缓有关,其主要表现为语言发育迟缓、行为问题和轻度的发育异常特征。
Hum Mutat. 2012 Apr;33(4):728-40. doi: 10.1002/humu.22037.
10
Wnt signaling in the murine diastema.Wnt 信号在小鼠牙间隙中的作用。
Eur J Orthod. 2012 Aug;34(4):518-24. doi: 10.1093/ejo/cjr049. Epub 2011 Apr 29.

Sox基因在牙齿发育中的表达。

Expression of Sox genes in tooth development.

作者信息

Kawasaki Katsushige, Kawasaki Maiko, Watanabe Momoko, Idrus Erik, Nagai Takahiro, Oommen Shelly, Maeda Takeyasu, Hagiwara Nobuko, Que Jianwen, Sharpe Paul T, Ohazama Atsushi

机构信息

Division of Oral Anatomy, Department of Oral Biological Science, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

出版信息

Int J Dev Biol. 2015;59(10-12):471-8. doi: 10.1387/ijdb.150192ao.

DOI:10.1387/ijdb.150192ao
PMID:26864488
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5292047/
Abstract

Members of the Sox gene family play roles in many biological processes including organogenesis. We carried out comparative in situ hybridization analysis of seventeen sox genes (Sox1-14, 17, 18, 21) during murine odontogenesis from the epithelial thickening to the cytodifferentiation stages. Localized expression of five Sox genes (Sox6, 9, 13, 14 and 21) was observed in tooth bud epithelium. Sox13 showed restricted expression in the primary enamel knots. At the early bell stage, three Sox genes (Sox8, 11, 17 and 21) were expressed in pre-ameloblasts, whereas two others (Sox5 and 18) showed expression in odontoblasts. Sox genes thus showed a dynamic spatio-temporal expression during tooth development.

摘要

Sox基因家族成员在包括器官发生在内的许多生物学过程中发挥作用。我们对17个sox基因(Sox1 - 14、17、18、21)在小鼠牙齿发生过程中从上皮增厚到细胞分化阶段进行了比较原位杂交分析。在牙胚上皮中观察到5个Sox基因(Sox6、9、13、14和21)的定位表达。Sox13在原发性釉结中表现出受限表达。在钟状早期阶段,3个Sox基因(Sox8、11、17和21)在成釉细胞前体细胞中表达,而另外2个(Sox5和18)在成牙本质细胞中表达。因此,Sox基因在牙齿发育过程中表现出动态的时空表达。