Profound obesity associated with a balanced translocation that disrupts the SIM1 gene

JL Holder Jr, NF Butte, AR Zinn - Human molecular genetics, 2000 - academic.oup.com
Human molecular genetics, 2000academic.oup.com
Studies of mice and humans have revealed a number of genes that when mutated result in
severe obesity. We have studied a unique girl with early-onset obesity and a de novo
balanced translocation between chromo‐somes 1p22. 1 and 6q16. 2. Her weight gain is
most likely due to excessive food intake, since measured energy expenditure was normal.
We cloned and sequenced both translocation breakpoints. The translocation does not
appear to affect any transcription unit on 1p, but it disrupts the SIM1 gene on 6q. SIM1 …
Abstract
Studies of mice and humans have revealed a number of genes that when mutated result in severe obesity. We have studied a unique girl with early-onset obesity and a de novo balanced translocation between chromo‐ somes 1p22.1 and 6q16.2. Her weight gain is most likely due to excessive food intake, since measured energy expenditure was normal. We cloned and sequenced both translocation breakpoints. The translocation does not appear to affect any transcription unit on 1p, but it disrupts the SIM1 gene on 6q. SIM1 encodes a human homolog of Drosophila Sim (Single-minded), a tran‐ scription factor involved in midline neurogenesis, and is a prototypical member of the bHLH-PAS (basic helix–loophelix + period, aryl hydrocarbon receptor, Single-minded) gene family. Our subject’s trans‐ location separates the 5′ promoter region and bHLH domain from the 3′ PAS and putative transcriptional regulation domains. The transcriptional targets of SIM1 are not known. Mouse Sim1 is expressed in the developing kidney and central nervous system, and is essential for formation of the supraoptic and paraventricular (PVN) nuclei of the hypothalamus. Previous neuroanatomical and pharmacological studies have implicated the PVN in the regulation of body weight: PVN neurons express the melanocortin 4 receptor and appear to be physiological targets of α-melanocyte-stimulating hormone, which inhibits food intake. We hypothesize that haploinsufficiency of SIM1, possibly acting upstream or downstream of the melanocortin 4 receptor in the PVN, is responsible for severe obesity in our subject.
Oxford University Press