Literature DB >> 21461901

B6-MSM consomic mouse strains reveal multiple loci for genetic variation in sucrose octaacetate aversion.

Ayako Ishii1, Tsuyoshi Koide, Aki Takahashi, Toshihiko Shiroishi, Thomas P Hettinger, Marion E Frank, Lawrence D Savoy, Bradley K Formaker, Sezen Yertutanol, Arimantas Lionikas, David A Blizard.   

Abstract

Based on crosses among inbred strains derived principally from M. m. domesticus, sucrose octaacetate (SOA) aversion in laboratory mice has been thought for many years to be controlled by a single genetic locus (Soa) located on distal chromosome (Chr) 6. To expand knowledge of the genetic basis underlying SOA aversion, we have studied the M. m. molossinus derived strain (MSM) and MSM consomic strains on a M. m. domesticus (C57BL/6J: B6) host background. Using two-bottle preference procedures, MSM mice avoided 0.1 mM and 1 mM SOA while B6 mice were indifferent to 0.1 mM and exhibited slight aversion to 1 mM SOA. Preference tests of 16 available consomic strains implicated Chr 2, 4 and 15 in SOA aversion in addition to the prominent effect of the known Soa locus on Chr 6 (implicated by study of two congenic strains). The originally defined Soa locus is presumably associated with one or more members of the cluster of Tas2r genes on distal Chr 6 that code for bitter taste receptors. Our results point to the possible role of established Tas2r genes on Chr 2 and 15, as well as to genes not coding for bitter receptors (Chr 4), in SOA aversion. SOA aversion emerges from this consomic screen as being definitively under polygenic control. The genetic diversity captured by the MSM model system is shown to be a valuable tool to complement the limited genetic variation in the commonly used stocks derived from M m. domesticus.

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Year:  2011        PMID: 21461901     DOI: 10.1007/s10519-011-9464-3

Source DB:  PubMed          Journal:  Behav Genet        ISSN: 0001-8244            Impact factor:   2.805


  5 in total

1.  Gene-trap mutagenesis using Mol/MSM-1 embryonic stem cells from MSM/Ms mice.

Authors:  Mai Nakahara; Hiroki Tateyama; Masatake Araki; Naomi Nakagata; Ken-ichi Yamamura; Kimi Araki
Journal:  Mamm Genome       Date:  2013-04-20       Impact factor: 2.957

2.  Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains.

Authors:  S Kato; A Ishii; A Nishi; S Kuriki; T Koide
Journal:  Heredity (Edinb)       Date:  2014-04-30       Impact factor: 3.821

3.  Baseline Muscle Mass Is a Poor Predictor of Functional Overload-Induced Gain in the Mouse Model.

Authors:  Audrius Kilikevicius; Lutz Bunger; Arimantas Lionikas
Journal:  Front Physiol       Date:  2016-11-15       Impact factor: 4.566

4.  Forced Running Endurance Is Influenced by Gene(s) on Mouse Chromosome 10.

Authors:  Mindaugas Kvedaras; Petras Minderis; Andrej Fokin; Aivaras Ratkevicius; Tomas Venckunas; Arimantas Lionikas
Journal:  Front Physiol       Date:  2017-01-23       Impact factor: 4.566

5.  Efficient genome editing in wild strains of mice using the i-GONAD method.

Authors:  Yuji Imai; Akira Tanave; Makoto Matsuyama; Tsuyoshi Koide
Journal:  Sci Rep       Date:  2022-08-15       Impact factor: 4.996

  5 in total

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