Sarcospan-deficient mouse as a model for clinical disorders associated with sarcospan mutations

A method for identifying a therapeutic agent for the treatment of an individual diagnosed with a metabolic disorder associated with a reduction or loss of expression of wild-type sarcospan in the individual, comprising:

• a) providing a transgenic knockout mouse whose genome comprises a homozygous disruption in its endogenous sarcospan gene, wherein said homozygous disruption prevents the expression of a functional sarcospan protein in cells of the mouse, wherein said homozygous disruption results in said transgenic knockout mouse exhibiting symptoms of a metabolic disorder selected from the group consisting of:
• larger epididymal fat deposits as compared to epididymal fat deposits of a wild-type mouse, larger intrascapular brown adipose tissue deposits as compared to the intrascapular brown adipose tissue deposits of a wild-type mouse, and increased body weight as compared to the body weight of a wild-type mouse;
• b) administering a candidate therapeutic agent to the transgenic knockout mouse of step a);
• and
• c) assaying the therapeutic effects of the candidate therapeutic agent by comparing the symptoms of the metabolic disorder in the transgenic knockout mouse which has received the candidate agent as in step b) with the symptoms of the metabolic disorder of a transgenic knockout mouse of step a) which has not received the candidate therapeutic agent, wherein amelioration of one or more of the symptoms of the metabolic disorder in the transgenic knockout mouse of step b) is an indication of the therapeutic effect of the candidate therapeutic agent.

A method for identifying an agent for reduction of weight gain in an individual wherein said weight gain is associated with a reduction or loss of expression of wild-type sarcospan in the individual, comprising:

• a) providing a transgenic knockout mouse whose genome comprises a homozygous disruption in its endogenous sarcospan gene, wherein said homozygous disruption prevents the expression of a functional sarcospan protein in cells of the mouse, wherein said homozygous disruption results in said transgenic knockout mouse exhibiting symptoms of a metabolic disorder selected from the group consisting of:
• larger epididymal fat deposits as compared to epididymal fat deposits of a wild-type mouse, larger intrascapular brown adipose tissue deposits as compared to the intrascapular brown adipose tissue deposits of a wild-type mouse, and increased body weight as compared to the body weight of a wild-type mouse;
• b) administering a candidate agent to the transgenic knockout mouse of step a);
• and
• c) assaying the effects of the candidate agent by comparing the fat pad or adipose deposits of the transgenic knockout mouse which has received the candidate agent as in step b) with the fat pad or adipose deposits of a transgenic knockout mouse of step a) which has received the candidate agent, wherein a reduction in the fat pad or adipose deposits in the transgenic knockout mouse of step b) is an indication that the agent has a reduction of weight gain effect in the individual.