Truncating Homozygous Mutation of Carboxypeptidase E (CPE) in a Morbidly Obese Female with Type 2 Diabetes Mellitus, Intellectual Disability and Hypogonadotrophic Hypogonadism

PLoS One. 2015 Jun 29;10(6):e0131417. doi: 10.1371/journal.pone.0131417. eCollection 2015.

Abstract

Carboxypeptidase E is a peptide processing enzyme, involved in cleaving numerous peptide precursors, including neuropeptides and hormones involved in appetite control and glucose metabolism. Exome sequencing of a morbidly obese female from a consanguineous family revealed homozygosity for a truncating mutation of the CPE gene (c.76_98del; p.E26RfsX68). Analysis detected no CPE expression in whole blood-derived RNA from the proband, consistent with nonsense-mediated decay. The morbid obesity, intellectual disability, abnormal glucose homeostasis and hypogonadotrophic hypogonadism seen in this individual recapitulates phenotypes in the previously described fat/fat and Cpe knockout mouse models, evidencing the importance of this peptide/hormone-processing enzyme in regulating body weight, metabolism, and brain and reproductive function in humans.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carboxypeptidase H / genetics*
  • Carboxypeptidase H / metabolism
  • DNA Mutational Analysis
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / enzymology
  • Diabetes Mellitus, Type 2 / genetics
  • Exome / genetics
  • Female
  • Gene Expression Regulation, Enzymologic
  • Homozygote
  • Humans
  • Intellectual Disability / complications*
  • Intellectual Disability / genetics
  • Klinefelter Syndrome / complications*
  • Klinefelter Syndrome / enzymology
  • Klinefelter Syndrome / genetics
  • Male
  • Mutation / genetics*
  • Obesity, Morbid / complications*
  • Obesity, Morbid / enzymology
  • Obesity, Morbid / genetics*
  • Pedigree
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Young Adult

Substances

  • RNA, Messenger
  • Carboxypeptidase H