Literature DB >> 10051320

Mapping and characterization of quantitative trait loci for non-insulin-dependent diabetes mellitus with an improved genetic map in the Otsuka Long-Evans Tokushima fatty rat.

S Wei1, K Wei, D H Moralejo, T Ogino, G Koike, H J Jacob, K Sugiura, Y Sasaki, T Yamada, K Matsumoto.   

Abstract

The Otsuka Long-Evans Tokushima Fatty (OLETF) rat is an animal model for obese-type, non-insulin-dependent diabetes mellitus (NIDDM) in humans. We have previously reported four quantitative trait loci (QTLs) responsible for NIDDM on Chromosomes (Chrs) 7, 14, 8, and 11 (Nidd1-4/of for Non-insulin-dependent diabetes1-4/oletf) by a whole-genome search in 160 F2 progenies obtained by mating the OLETF and the Fischer-344 (F344) rats. Our present investigation was designed to identify and characterize novel QTLs affecting NIDDM by performing a genome-wide linkage analysis of genes for glucose levels and body weight and analysis for gene-to-gene and gene-to-body-weight interactions on an improved genetic map with a set of 382 informative markers in the 160 F2 progenies. We have identified seven novel QTLs on rat Chrs 1 (Nidd5 and 6/of), 5 (Nidd7/of), 9 (Nidd8/of), 12 (Nidd9/of), 14 (Nidd10/of) and 16 (Nidd11/of) which, together with the Nidd1-4/of, account for a total of approximately 60% and approximately 75% of the genetic variance of the fasting and postprandial glucose levels, respectively, in the F2. While the OLETF allele corresponds with increased glucose levels as expected for the novel QTLs except Nidd8 and 9/of, the Nidd8 and 9/of exhibit heterosis: heterozygotes showing significantly higher glucose levels than OLETF or F344 homozygotes. There are epistatic interactions between Nidd1 and 10/of and between Nidd2 and 8/of. Additionally, our results indicated that the Nidd6 and 11/of could also contribute to an increase of body weight, and that the other five QTLs could show no linkage with body weight, but Nidd8,9, and 10/of have an interaction with body weight.

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Year:  1999        PMID: 10051320     DOI: 10.1007/s003359900982

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  16 in total

Review 1.  Defining the genetic contribution of type 2 diabetes mellitus.

Authors:  J van Tilburg; T W van Haeften; P Pearson; C Wijmenga
Journal:  J Med Genet       Date:  2001-09       Impact factor: 6.318

2.  Identification of candidate disease genes by EST alignments, synteny, and expression and verification of Ensembl genes on rat chromosome 1q43-54.

Authors:  Ursula Vitt; Darryl Gietzen; Kristian Stevens; Jim Wingrove; Shanya Becha; Sean Bulloch; John Burrill; Narinder Chawla; Jennifer Chien; Matthew Crawford; Craig Ison; Liam Kearney; Mary Kwong; Joe Park; Jennifer Policky; Mark Weiler; Renee White; Yuming Xu; Sue Daniels; Howard Jacob; Michael I Jensen-Seaman; Jozef Lazar; Laura Stuve; Jeanette Schmidt
Journal:  Genome Res       Date:  2004-04       Impact factor: 9.043

3.  Mapping of genetic loci predisposing to hypertriglyceridaemia in the hereditary hypertriglyceridaemic rat: analysis of genetic association with related traits of the insulin resistance syndrome.

Authors:  I Klimes; K Weston; P Kovacs; D Gasperikova; D Jezova; R Kvetnansky; J R Thompson; E Sebokova; N J Samani
Journal:  Diabetologia       Date:  2003-03-01       Impact factor: 10.122

4.  New animal models reveal that coenzyme Q2 (Coq2) and placenta-specific 8 (Plac8) are candidate genes for the onset of type 2 diabetes associated with obesity in rats.

Authors:  Daiki Sasaki; Jun Kotoh; Risa Watadani; Kozo Matsumoto
Journal:  Mamm Genome       Date:  2015-08-22       Impact factor: 2.957

5.  Genetic variation in aldosterone synthase predicts plasma glucose levels.

Authors:  K Ranade; K D Wu; N Risch; M Olivier; D Pei; C F Hsiao; L M Chuang; L T Ho; E Jorgenson; R Pesich; Y D Chen; V Dzau; A Lin; R A Olshen; D Curb; D R Cox; D Botstein
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-30       Impact factor: 11.205

6.  Major quantitative trait locus on chromosome 2 for glucose tolerance in diabetic SMXA-5 mouse established from non-diabetic SM/J and A/J strains.

Authors:  M Kobayashi; F Io; T Kawai; M Kumazawa; H Ikegami; M Nishimura; T Ohno; F Horio
Journal:  Diabetologia       Date:  2006-01-31       Impact factor: 10.122

7.  Epistasis between hyperglycemic QTLs revealed in a double congenic of the OLETF rat.

Authors:  Hiroyuki Kose; Yoshimi Bando; Keisuke Izumi; Takahisa Yamada; Kozo Matsumoto
Journal:  Mamm Genome       Date:  2007-08-21       Impact factor: 2.957

8.  Fine-mapping a locus for glucose tolerance using heterogeneous stock rats.

Authors:  Leah C Solberg Woods; Katie Holl; Michael Tschannen; William Valdar
Journal:  Physiol Genomics       Date:  2010-01-12       Impact factor: 3.107

9.  Normal feeding and body weight in Fischer 344 rats lacking the cholecystokinin-1 receptor gene.

Authors:  J E Blevins; J Overduin; J M Fuller; D E Cummings; K Matsumoto; D H Moralejo
Journal:  Brain Res       Date:  2008-12-16       Impact factor: 3.252

10.  Fine-mapping diabetes-related traits, including insulin resistance, in heterogeneous stock rats.

Authors:  Leah C Solberg Woods; Katie L Holl; Daniel Oreper; Yuying Xie; Shirng-Wern Tsaih; William Valdar
Journal:  Physiol Genomics       Date:  2012-09-04       Impact factor: 3.107

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