Novel LEPR mutations in obese Pakistani children identified by PCR‐based enrichment and next generation sequencing
Objective Mutations in leptin receptor gene (LEPR) result in early onset extreme adiposity. However, their prevalence in different populations is not known. Indeed, LEPR screening by gold standard Sanger sequencing has been limited by its large size and the cost. One‐step PCR‐based targeted enrichme...
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Veröffentlicht in: | Obesity (Silver Spring, Md.) Md.), 2014-04, Vol.22 (4), p.1112-1117 |
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Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Objective
Mutations in leptin receptor gene (LEPR) result in early onset extreme adiposity. However, their prevalence in different populations is not known. Indeed, LEPR screening by gold standard Sanger sequencing has been limited by its large size and the cost. One‐step PCR‐based targeted enrichment could be an option for rapid and cost effective molecular diagnosis of monogenic forms of obesity.
Methods
The study is based on 39 unrelated severely obese Pakistani children, previously shown to be negative for leptin (LEP) and melanocortin 4 receptor (MC4R) gene mutations, from an initial cohort of 62 probands. Patient samples were analyzed by microdroplet PCR‐enrichment (RainDance technologies) targeting coding exons of 26 obesity‐associated genes combined with next generation sequencing. Hormone levels were analyzed by ELISA.
Results
The analysis revealed two novel homozygous LEPR mutations, an essential splice site mutation in exon 15 (c.2396‐1 G>T), and a nonsense mutation in exon 10 (c.1675 G>A). Both probands had high leptin levels and were phenotypically indistinguishable from age‐matched leptin‐deficient subjects from the same population.
Conclusions
The two subjects carrying homozygous LEPR mutations, reported here for the first time in the Pakistani population, constitute 3% of the whole cohort of severely obese children (compared to 17% for LEP and 3% for MC4R). |
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ISSN: | 1930-7381 1930-739X |
DOI: | 10.1002/oby.20667 |