Nicotinamide Nucleotide Transhydrogenase (Nnt) is Related to Obesity in Mice

Abstract The C57BL/6J (B6J) mouse strain has been widely used as a control strain for the study of metabolic diseases and diet induced obesity (DIO). B6J mice carry a spontaneous deletion mutation in the nicotinamide nucleotide transhydrogenase (Nnt) gene eliminating exons 7–11, resulting in expression of a truncated form of Nnt, an enzyme that pumps protons across the inner mitochondrial membrane. It has been proposed that this mutation in B6J mice is associated with epigonadal fat mass and altered sensitivity to diet induced obesity. To define the role of Nnt in the development of diet induced obesity, we generated first backcross (BC1) hybrids of wild type Nnt C57BL/6NTac and mutated Nnt C57BL/6JRj [(C57BL/6NTac×C57BL/6JRj)F1×C57BL/6NTac]. Body weight gain and specific fat-pad depot mass were measured in BC1 hybrids under high fat diet conditions. Both sexes of BC1 hybrids indicate that mice with Nnt wild type allele are highly sensitive to DIO and exhibit higher relative fat mass. In summary, our data indicate that the Nnt mutation in mice is associated with sensitivity to DIO and fat mass.

[1]  R. Hull,et al.  High fat feeding unmasks variable insulin responses in male C57BL/6 mouse substrains. , 2017, The Journal of endocrinology.

[2]  Manisha N. Patel,et al.  Nicotinamide Nucleotide Transhydrogenase (Nnt) Links the Substrate Requirement in Brain Mitochondria for Hydrogen Peroxide Removal to the Thioredoxin/Peroxiredoxin (Trx/Prx) System* , 2014, The Journal of Biological Chemistry.

[3]  M. Stumvoll,et al.  Nicotinamide nucleotide transhydrogenase mRNA expression is related to human obesity , 2013, Obesity.

[4]  E. Cadenas,et al.  Silencing of nicotinamide nucleotide transhydrogenase impairs cellular redox homeostasis and energy metabolism in PC12 cells. , 2012, Biochimica et biophysica acta.

[5]  M. Stumvoll,et al.  C57BL/6JRj mice are protected against diet induced obesity (DIO). , 2012, Biochemical and biophysical research communications.

[6]  F. Pazos,et al.  Genetic polymorphisms among C57BL/6 mouse inbred strains , 2011, Transgenic Research.

[7]  E. Leiter,et al.  Diet‐induced Obesity in Two C57BL/6 Substrains With Intact or Mutant Nicotinamide Nucleotide Transhydrogenase (Nnt) Gene , 2010, Obesity.

[8]  A. Yoshiki,et al.  Genetic differences among C57BL/6 substrains. , 2009, Experimental animals.

[9]  G. Morahan,et al.  Increased nicotinamide nucleotide transhydrogenase levels predispose to insulin hypersecretion in a mouse strain susceptible to diabetes , 2007, Diabetologia.

[10]  M. Fasshauer,et al.  Serum retinol-binding protein is more highly expressed in visceral than in subcutaneous adipose tissue and is a marker of intra-abdominal fat mass. , 2007, Cell metabolism.

[11]  F. Ashcroft,et al.  Deletion of Nicotinamide Nucleotide Transhydrogenase , 2006, Diabetes.

[12]  J. Rydström Mitochondrial transhydrogenase--a key enzyme in insulin secretion and, potentially, diabetes. , 2006, Trends in biochemical sciences.

[13]  F. Ashcroft,et al.  A genetic and physiological study of impaired glucose homeostasis control in C57BL/6J mice , 2005, Diabetologia.

[14]  Yueming Ding,et al.  An efficient SNP system for mouse genome scanning and elucidating strain relationships. , 2004, Genome research.

[15]  R. Surwit,et al.  Genetic vulnerability to diet-induced obesity in the C57BL/6J mouse: physiological and molecular characteristics , 2004, Physiology & Behavior.

[16]  William H. Majoros,et al.  A Comparison of Whole-Genome Shotgun-Derived Mouse Chromosome 16 and the Human Genome , 2002, Science.

[17]  J. Hoek,et al.  Physiological roles of nicotinamide nucleotide transhydrogenase. , 1988, The Biochemical journal.

[18]  G. Morahan,et al.  The deletion variant of nicotinamide nucleotide transhydrogenase (Nnt) does not affect insulin secretion or glucose tolerance. , 2010, Endocrinology.