Suppr超能文献

异常的切牙形态表明Tfap2a和Tfap2b在牙齿发育中具有组织特异性作用。

Anomalous incisor morphology indicates tissue-specific roles for Tfap2a and Tfap2b in tooth development.

作者信息

Woodruff Emily D, Gutierrez Galaxy C, Van Otterloo Eric, Williams Trevor, Cohn Martin J

机构信息

Department of Biology, University of Florida, Gainesville, FL, USA.

Department of Biology, University of Florida, Gainesville, FL, USA.

出版信息

Dev Biol. 2021 Apr;472:67-74. doi: 10.1016/j.ydbio.2020.12.017. Epub 2021 Jan 15.

Abstract

Mice possess two types of teeth that differ in their cusp patterns; incisors have one cusp and molars have multiple cusps. The patterning of these two types of teeth relies on fine-tuning of the reciprocal molecular signaling between dental epithelial and mesenchymal tissues during embryonic development. The AP-2 transcription factors, particularly Tfap2a and Tfap2b, are essential components of such epithelial-mesenchymal signaling interactions that coordinate craniofacial development in mice and other vertebrates, but little is known about their roles in the regulation of tooth development and shape. Here we demonstrate that incisors and molars differ in their temporal and spatial expression of Tfap2a and Tfap2b. At the bud stage, Tfap2a is expressed in both the epithelium and mesenchyme of the incisors and molars, but Tfap2b expression is restricted to the molar mesenchyme, only later appearing in the incisor epithelium. Tissue-specific deletions show that loss of the epithelial domain of Tfap2a and Tfap2b affects the number and spatial arrangement of the incisors, notably resulting in duplicated lower incisors. In contrast, deletion of these two genes in the mesenchymal domain has little effect on tooth development. Collectively these results implicate epithelial expression of Tfap2a and Tfap2b in regulating the extent of the dental lamina associated with patterning the incisors and suggest that these genes contribute to morphological differences between anterior (incisor) and posterior (molar) teeth within the mammalian dentition.

摘要

小鼠有两种牙尖模式不同的牙齿;门牙有一个牙尖,臼齿有多个牙尖。这两种牙齿的模式形成依赖于胚胎发育过程中牙上皮和间充质组织之间相互分子信号的微调。AP-2转录因子,特别是Tfap2a和Tfap2b,是这种上皮-间充质信号相互作用的重要组成部分,它们协调小鼠和其他脊椎动物的颅面发育,但对它们在牙齿发育和形状调节中的作用知之甚少。在这里,我们证明门牙和臼齿在Tfap2a和Tfap2b的时空表达上存在差异。在芽期,Tfap2a在门牙和臼齿的上皮和间充质中均有表达,但Tfap2b的表达仅限于臼齿间充质,随后才出现在门牙上皮中。组织特异性缺失表明,Tfap2a和Tfap2b上皮结构域的缺失会影响门牙的数量和空间排列,特别是导致下门牙重复。相比之下,在间充质结构域中删除这两个基因对牙齿发育影响不大。这些结果共同表明,Tfap2a和Tfap2b的上皮表达在调节与门牙模式形成相关的牙板范围中起作用,并表明这些基因有助于哺乳动物牙列中前牙(门牙)和后牙(臼齿)之间的形态差异。

相似文献

1
Anomalous incisor morphology indicates tissue-specific roles for Tfap2a and Tfap2b in tooth development.
Dev Biol. 2021 Apr;472:67-74. doi: 10.1016/j.ydbio.2020.12.017. Epub 2021 Jan 15.
2
Transcriptional programs of Pitx2 and Tfap2a/Tfap2b controlling lineage specification of mandibular epithelium during tooth initiation.
PLoS Genet. 2024 Jul 25;20(7):e1011364. doi: 10.1371/journal.pgen.1011364. eCollection 2024 Jul.
3
Expression and function of FGFs-4, -8, and -9 suggest functional redundancy and repetitive use as epithelial signals during tooth morphogenesis.
Dev Dyn. 1998 Mar;211(3):256-68. doi: 10.1002/(SICI)1097-0177(199803)211:3<256::AID-AJA7>3.0.CO;2-G.
6
Tooth-type specific expression of dHAND/Hand2: possible involvement in murine lower incisor morphogenesis.
Cell Tissue Res. 2002 Nov;310(2):201-12. doi: 10.1007/s00441-002-0611-2. Epub 2002 Sep 14.
7
Spatiotemporal expression of the homeobox gene S8 during mouse tooth development.
Arch Oral Biol. 1997 Sep;42(9):625-31. doi: 10.1016/s0003-9969(97)00057-5.
8
Noggin is required for early development of murine upper incisors.
J Dent Res. 2012 Apr;91(4):394-400. doi: 10.1177/0022034511435939. Epub 2012 Feb 2.
9
Associations of FGF-3 and FGF-10 with signaling networks regulating tooth morphogenesis.
Dev Dyn. 2000 Nov;219(3):322-32. doi: 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1062>3.0.CO;2-J.
10
Ectopic Activation of in Dental Mesenchyme Causes Incisor Agenesis and Molar Microdontia.
Int J Mol Sci. 2024 Jun 27;25(13):7045. doi: 10.3390/ijms25137045.

本文引用的文献

1
AP-2β/KCTD1 Control Distal Nephron Differentiation and Protect against Renal Fibrosis.
Dev Cell. 2020 Aug 10;54(3):348-366.e5. doi: 10.1016/j.devcel.2020.05.026. Epub 2020 Jun 17.
2
Heterodimerization of TFAP2 pioneer factors drives epigenomic remodeling during neural crest specification.
Genome Res. 2020 Jan;30(1):35-48. doi: 10.1101/gr.249680.119. Epub 2019 Dec 17.
3
4
TFAP2B mutation and dental anomalies.
J Hum Genet. 2017 Aug;62(8):769-775. doi: 10.1038/jhg.2017.37. Epub 2017 Apr 6.
5
A tissue-specific role for intraflagellar transport genes during craniofacial development.
PLoS One. 2017 Mar 27;12(3):e0174206. doi: 10.1371/journal.pone.0174206. eCollection 2017.
6
TFAP2 paralogs regulate melanocyte differentiation in parallel with MITF.
PLoS Genet. 2017 Mar 1;13(3):e1006636. doi: 10.1371/journal.pgen.1006636. eCollection 2017 Mar.
8
Genome-wide analysis of gene expression in human embryonic tooth germ.
J Mol Histol. 2014 Dec;45(6):609-17. doi: 10.1007/s10735-014-9580-5. Epub 2014 Aug 5.
9
Identification and dissection of a key enhancer mediating cranial neural crest specific expression of transcription factor, Ets-1.
Dev Biol. 2013 Oct 15;382(2):567-75. doi: 10.1016/j.ydbio.2013.08.009. Epub 2013 Aug 19.
10
Morphology and chronology of diphyodont dentition in miniature pigs, Sus Scrofa.
Oral Dis. 2014 May;20(4):367-79. doi: 10.1111/odi.12126. Epub 2013 May 16.

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