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・ Sim Van der Ryn
・ Sim Var
・ Sim Visser
・ Sim Walton
・ Sim Wong Hoo
・ Sim Woo-yeon
・ Sim Yee Chiang
・ Sim Yunkyung
・ Sim's Park, Coonoor
・ Sim, Chelyabinsk Oblast
・ Sim, Perm Krai
・ Sim, Russia
・ Sim-Feng Shui
・ SIM-II
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SIM1
・ SIM2
・ Sim4
・ SIMA
・ Sima
・ Sima (architecture)
・ Sima (Chinese surname)
・ Sima (geology)
・ Sima (given name)
・ Sima (mead)
・ Sima (office)
・ Sima Ai
・ Sima Ang
・ Sima Avramović
・ Sima Babovich


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SIM1 : ウィキペディア英語版
SIM1

Single-minded homolog 1 also known as class E basic helix-loop-helix protein 14 (bHLHe14) is a protein that in humans is encoded by the ''SIM1'' gene.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6492 )
== Function ==

SIM1 and SIM2 genes are homologs of ''Drosophila melanogaster'' single-minded (sim), so named because cells in the midline of the sim mutant embryo fail to properly develop and eventually die, and thus the paired longitudinal axon bundles that span the anterior-posterior axis of the embryo (analogous to the embryo's spinal cord) are collapsed into a "single" rudimentary axon bundle at the midline. Sim is a basic helix-loop-helix-PAS domain transcription factor that regulates gene expression in the midline cells. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis, it was proposed that the human SIM2 gene, which resides in a critical region of chromosome 21, is a candidate for involvement in certain dysmorphic features (particularly facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.〔
Haploinsufficiency of SIM1 has been shown to cause severe early-onset obesity in a human girl with a de novo balanced translocation between chromosomes 1p22.1 and 6q16.2 and has been suggested to cause a Prader-Willi-like phenotype in other cases. Additionally, studies in mice have shown that haploinsufficieny of Sim1 causes obesity that is due to hyperphagia and do not respond properly to increased dietary fat.〔 Overexpression of SIM1 protects against diet induced obesity and rescues the hyperphagia of agouti yellow mice, who have disrupted melanocortin signaling. The obesity and hyperphagia may be mediated by impaired melanocortin activation of PVN neurons and oxytocin deficiency in these mice. It has been demonstrated that modulating Sim1 levels postnatally also leads to hyperphagia and obesity, suggesting a physiological role for Sim1 separate from its role in development.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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