期刊文献+

DLX1基因在人牙齿发育中的表达 被引量:1

Expression of DLX1 Gene in the Human Embryonic Tooth Germ
下载PDF
导出
摘要 目的:研究DLX1基因在人牙齿发育中的表达模式,确定DLX1转录子亚型。方法:提取人牙胚总RNA,利用巢式RT-PCR技术克隆DLX1cDNA序列;制备地高辛标记的RNA探针,检测人磨牙发育不同时期DLX1的表达情况。结果:人牙胚中表达的DLX1为转录子亚型1。在表达模式上,11周、14周、17周和19周4个不同发育时期磨牙均有DLX1表达,11周和14周少量表达于牙上皮和间充质,17周依然在牙上皮和间充质中表达,但表达增强,19周表达主要集中在内釉上皮细胞。结论:DLX1在人牙齿发育的各个时期均有表达,表明DLX1可能是人类牙齿发育中的一个重要调节因子。 Objective: To examine the expression pattern and determine the transcript variant of DLX1 gene in the human embryonic tooth germ. Methods: DLX1 cDNA fragment was cloned from the human developing tooth germ by nested RT--PCR. The expression patterns of DLX1 gene at multiple molar developing stages (11W, 14W, 17W and 19W) were examined using biotin--labelled in situ hybridization. Results: DLX1 gene expressed at human tooth germ is transcript variant 1. Weak expression of DLX1 was detected in the dental epithelium and the dental mesenchyme at 11W and 14W, which increased at 17W. At 19W, expression of DLX1 was only restricted in the inner en- amel epithelium. Conclusion: Expression of DLX1 was detected in multiple developing stages of molar, indicating that DLX1 may be a critical regulation factor in human tooth development.
出处 《口腔医学研究》 CAS CSCD 2014年第6期497-499,503,共4页 Journal of Oral Science Research
基金 国家自然科学青年基金(编号:81200761) 福建省教育厅重点项目(编号:JA12061) 福建省自然科学基金项目(编号:2011J01146)
关键词 DLX1基因 牙齿发育 基因表达 DLX1 gene Tooth development Gene expression
  • 相关文献

参考文献11

  • 1Thomas BL, Tucker AS, Qui M, et al. Role of Dlx- 1 and Dlx-2 genes in patterning of the routine dentition [J]. De- velopment,1997,124(23) : 4811 -8.
  • 2Zerucha T, and M Ekker. Distal-less-related homeobox genes of vertebrates; evolution, function, and regulation [J]. BiochemCell Biol,2000,78(5) : 593-601.
  • 3I.ezot F, Thomas B, Greene SR, et al. Physiological implica- tions of DLX homeoproteins in enamel formation [J]. J Cell Physiol,2008,216(3) : 688-97.
  • 4Qiu M, Bulfone A, Ghaltas I, el al. Role of the Dlx ho- meobox genes in proximodistal patterning of the branchial ar- ches: mutations of Dlx- 1, Dlx-2, and Dlx- 1 and - 2 al- ter morpbogenesis of proximal skeletal and soft tissue strue lures derived from the first and second arches [J]. Dev Biol, 1997, 185(2) : 165 -84.
  • 5Park BK, Sperber SM, Choudhury A, el al. lntergenic en- hancers with distinct activities regulate Dlx gene expression in the mesenchyme of the branchial arches [J]. Developmental biology, 2004, 268(2) : 532- 545.
  • 6McKinsey GL, I.indmer S, Trzcinski B, et al. Dlxl &2- de- pendent expression of Zfhxlb (Sipl , Zeb2) regulates the fate switch between cortical and striatal interneurons [J]. Neu- ron, 2013, 77(1) : 83-98.
  • 7Ghosh AK, Shankar DB, Shackleford GM, et al. Molecular cloning and characterization of human FGF8 ahernalive mes- senger RNA forms [J]. Cell Growth Differ, 1996, 7(10) : 1425-34.
  • 8Zhang Y, Zhao X, Hu Y, et al. Msxl is required for the in- duction of Patched by Sonic hedgehog in the mammalian tooth germ [J]. DevDyn, 1999, 215(1) : 45-53.
  • 9Cohen SM, G Jürgens, Proximal-distal pattern [ormation in Drosophila: cell autonomous requirement for Distal- less gene activity in limb development [J]. The EMBO journal, 1989, 8(7) : 2045.
  • 10孙昊,姜文辉,王旭东.Dlx1/Dlx2基因对小鼠第一鳃弓发育调控机制的研究进展[J].中华口腔医学研究杂志(电子版),2010,4(1):56-59. 被引量:1

同被引文献16

  • 1Ron D, Habener JF. CHOP, a novel developmentally regula- ted nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative in- hibitor of gene transcription [J]. Genes Dev, 1992, 6(3) 439-53.
  • 2Ubeda M, Wang XZ, Zinszner H, et al. Stress-induced binding of the transcript- tional factor CHOP to a novel DNA control element [J]. Mol Cell Biol, 1996, 16(4) : 1479 -89.
  • 3Wang XZ, Lawson B, Brewer JW, et al. Signals from the stressed endoplasmic reticulum induce C/EBP-homologous protein (CHOP/GADD153) [J]. Mol Cell Biol, 1996, 16(8) 4273-80.
  • 4Fornace AJ Jr, Alamo I Jr, Hollander MC. DNA damage- inducible transcripts in mammalian cells [J]. Proe Natl Acad Sci U S A, 1988, 85(23) : 8800-4.
  • 5Brookes SJ, Barron MJ, Boot-Handford R, et al. Endo- plasmic reticulum stress in amelogenesis imperfecta and phe-.notypic rescue using 4-phenylbutyrate [J]. Hum Mol Gen- et, 2014, 23(9) : 2468-80.
  • 6Chen Y, Zhang Y, Ramachandran A,et al. DSPP Is Essential for Normal Develop-ment of the Dental-Craniofacial Com- plex [J]. J Dent Res, 2015 Oct 26. pii: 0022034515610768.
  • 7Mitsui SN, Yasue A, Masuda K, et al. Novel PAX9 muta- tions cause non-syndromic tooth agenesis I-J]. J Dent Res, 2014, 93(3) :245-9.
  • 8Li J, Feng J, Liu Y, et al. BMP-SHH signaling network controls epithelial stem cell fate via regulation of its niche in the developing tooth [J]. Dev Cell, 2015, 33(2) : 125-35.
  • 9Wang Q, Groenendyk J, Michalak M. Glycoprotein Quality Control and Endo- plasmic Reticulum Stress [J]. Mole- cules, 2015, 20(8) : 13689-704.
  • 10Xu S, Nam SM, Kim JH, et al. Palmitate induces ER calci- um depletion and apoptosis in mouse podocytes subsequent to mitochondrial oxidative stress [J]. Cell Death Dis, 2015, 6 : e1976.

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部