在OLETF大鼠中,< 1.7 cM间隔是导致Dmo1肥胖表型的原因。

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Takeshi K Watanabe, Shiro Okuno, Yuki Yamasaki, Toshihide Ono, Keiko Oga, Ayako Mizoguchi-Miyakita, Hideo Miyao, Mikio Suzuki, Hiroshi Momota, Yoshihiro Goto, Hiroichi Shinomiya, Haretsugu Hishigaki, Isamu Hayashi, Toshihiro Asai, Shigeyuki Wakitani, Toshihisa Takagi, Yusuke Nakamura, Akira Tanigami
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引用次数: 5

摘要

1. Dmo1 (Diabetes Mellitus OLETF type I)是雄性大鼠血脂异常、肥胖和糖尿病表型的主要数量性状位点。2. 我们通过将非糖尿病褐挪威(BN)大鼠的Dmo1染色体片段转移到OLETF菌株中产生的基因系证实了Dmo1在第四代(BC4)和第五代(BC5)基因动物中对血脂异常、肥胖和糖尿病的强大、广泛的治疗作用。对相对较少数量的BC5大鼠(n = 71)的分析表明,Dmo1的临界间隔位于D1Rat461和D1Rat459之间< 4.9 cM的区域。3.为了确认Dmo1临界区间的分配,我们对BC5动物进行交叉杂交以产生更大的研究群体(BC5:F1雄性;N = 406)。在本研究中,我们使用18周龄的体重作为肥胖指数;这种表型是密切相关的血脂异常和高血糖表型的代表。4. 区间映射在D1Rat90标记(LOD = 9.11)处分配了概率对数(LOD)峰值。一个LOD支持间隔位于D1Rat461和D1Rat459之间< 1.7 cM的区域内。5. 这项大型交叉研究证实,Dmo1可能局限于这一区间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A < 1.7 cM interval is responsible for Dmo1 obesity phenotypes in OLETF rats.

1. Dmo1 (Diabetes Mellitus OLETF type I) is a major quantitative trait locus for dyslipidaemia, obesity and diabetes phenotypes of male Otsuka Long Evans Tokushima Fatty (OLETF) rats. 2. Our congenic lines, produced by transferring Dmo1 chromosomal segments from the non-diabetic Brown Norway (BN) rat into the OLETF strain, have confirmed the strong, wide-range therapeutic effects of Dmo1 on dyslipidaemia, obesity and diabetes in the fourth (BC4) and fifth (BC5) generations of congenic animals. Analysis of a relatively small number of BC5 rats (n = 71) suggested that the critical Dmo1 interval lies within a < 4.9 cM region between D1Rat461 and D1Rat459. 3. To confirm the assignment of the Dmo1 critical interval, we intercrossed BC5 animals to produce a larger study population (BC5:F1 males; n = 406). For the present study, we used bodyweight at 18 weeks of age as an index of obesity; this phenotype is representative of the closely associated dyslipidaemia and hyperglycaemia phenotypes. 4. Interval mapping assigned logarithm of odds (LOD) peaks at the D1Rat90 marker (LOD = 9.11). One LOD support interval lies within the < 1.7 cM region between D1Rat461 and D1Rat459. 5. This large intercross study confirms that Dmo1 is likely localized within the interval.

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来源期刊
Clinical and Experimental Pharmacology and Physiology
Clinical and Experimental Pharmacology and Physiology PHARMACOLOGY & PHARMACY-PHYSIOLOGY
自引率
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128
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
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