Mapping of a Gene Causing Mouse Hypodontia to Chromosome 13

Kazuyuki Saito, Y. Asada
{"title":"Mapping of a Gene Causing Mouse Hypodontia to Chromosome 13","authors":"Kazuyuki Saito, Y. Asada","doi":"10.2330/JORALBIOSCI1965.43.690","DOIUrl":null,"url":null,"abstract":"The purpose of this study was to identify the major candidate chromosome and to detect the region that included the candidate gene (s) causing absence of the third molars in EL/sea mice. The candidate chromosomal analysis was performed on genetic crosses using two strains of mice, EL with absence of the third molars, and DDY with a normal complement of teeth. Linkage analysis by interval mapping with microsatellite markers suggested that mouse chromosome 13 was one of the candidate chromosomes and therefore this chromosome was investigated in detail by individual genotyping of F 2 intercross mice with missing third molars. The highest scores were found at D13Mit78 and D13Mit35 markers (xx2=11.8, p< 0.01). Based on these findings, it is suggested that the gene causing absent third molars in EL mice maps close to these microsatellite loci.","PeriodicalId":14631,"journal":{"name":"Japanese Journal of Oral Biology","volume":"4 1","pages":"690-699"},"PeriodicalIF":0.0000,"publicationDate":"2001-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese Journal of Oral Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2330/JORALBIOSCI1965.43.690","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The purpose of this study was to identify the major candidate chromosome and to detect the region that included the candidate gene (s) causing absence of the third molars in EL/sea mice. The candidate chromosomal analysis was performed on genetic crosses using two strains of mice, EL with absence of the third molars, and DDY with a normal complement of teeth. Linkage analysis by interval mapping with microsatellite markers suggested that mouse chromosome 13 was one of the candidate chromosomes and therefore this chromosome was investigated in detail by individual genotyping of F 2 intercross mice with missing third molars. The highest scores were found at D13Mit78 and D13Mit35 markers (xx2=11.8, p< 0.01). Based on these findings, it is suggested that the gene causing absent third molars in EL mice maps close to these microsatellite loci.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
致小鼠下颌畸形的13号染色体基因定位
本研究的目的是确定主要的候选染色体,并检测包含导致EL/海鼠第三磨牙缺失的候选基因的区域。候选染色体分析使用两种小鼠进行遗传杂交,EL缺失第三磨牙,DDY缺失正常牙齿。利用微卫星标记进行区间定位的连锁分析表明,小鼠13号染色体是缺失第三磨牙的候选染色体之一,因此我们对缺失第三磨牙的f2杂交小鼠进行了个体基因分型研究。D13Mit78和D13Mit35标记得分最高(xx2=11.8, p< 0.01)。基于这些发现,我们认为导致EL小鼠第三磨牙缺失的基因与这些微卫星位点接近。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Effect of Experimental Traumatic Occlusion on Temporomandibular Joint Changes of the Rat Dentin Matrix Proteins Affected by Long-term Administration of Hydroxyethylidene-1,1-bisphosphonate (HEBP). Alteration of the Expression of A 2 a Adenosine Receptor and Toll-like Receptor 4 in Macrophage Cell Lines Orientation of the Deep Part of the Human Temporal Muscle and Morphological Study of the Infratemporal Crest. Effects of Clenbuterol, a β2-adrenergic Agonist, on the Myofiber Diameter, Fiber Type, and Expressions of Insulin-like Growth Factors in the Adult Mouse Masseter Muscle
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1