维普中文期刊产品整合服务

Large-scale screening of disease model through ENU mutagenesis in mice

查看全文 作  者:[1]HEFang;[2]WANGZixing;[1]ZHAOJing;[1]BAOJie;[1]DINGJun;[1]RUANHaibin;[1]XIEQing;[3]ZHANGZuoming;[1]GAOXiang 高影响力作者 机构地区:[1]ModelAnimalResearchCenter,NanjingUniversity,Nanjing210093,China;[2]StateKeyLaboratoryofPharmaceuticalBiotechnology,NanjingUniversity,Nanjing210093,China;[3]DepartmentofAviationMedicine,FourthPLAMedicineUniversity,Xi'an710032,China高影响力机构 出  处:《Chinese Science Bulletin》索引2003年第48卷第24期,共7页高影响力期刊 基  金:supported by the State“863”High-Tech Project and the National Gongguan Project 摘  要:Manipulation of mouse genome has merged as one of the most important approaches for studying genefunction and establishing the disease model because of the high homology between human genome and mouse genome. In this study, the chemical mutagen ethylnitrosourea (ENU) was employed for inducing germ cell mutations in maleC57BL/6J mice. The first generation (G1) of the backcrossof these mutated mice, totally 3172, was screened for abnor-mal phenotypes on gross morphology, behavior, learning and memory, auditory brainstem response (ABR), electrocardio-gram (ECG), electroretinogram (ERG), flash-visual evoked potential (F-VEP), bone mineral density, and blood sugarlevel. 595 mice have been identified with specific dominantabnormalities. Fur color changes, eye defects and hearing loss occurred at the highest frequency. Abnormalities related to metabolism alteration are least frequent. Interestingly, eye defects displayed significant left-right asymmetry and sexpreference. Sex preference is also observed in mice with ab-normal bone mineral density. Among 104 G1 generation mutant mice examined for inheritability, 14 of them have been confirmed for passing abnormal phenotypes to their progenies. However, we did not observe behavior abnormali-ties of G1 mice to be inheritable, suggesting multi-gene con-trol for these complicated functions in mice. In conclusion, the generation of these mutants paves the way for under-standing molecular and cellular mechanisms of these ab-normal phenotypes, and accelerates the cloning of disease-related genes. 关 键 词:ENU 基因突变 染色体 形态学 心电图
相关文献

参考文献(12)

引证文献(1)

耦合文献(16)

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费