Literature DB >> 16955138

Severe facial clefting in Insig-deficient mouse embryos caused by sterol accumulation and reversed by lovastatin.

Luke J Engelking1, Bret M Evers, James A Richardson, Joseph L Goldstein, Michael S Brown, Guosheng Liang.   

Abstract

Insig-1 and Insig-2 are regulatory proteins that restrict the cholesterol biosynthetic pathway by preventing proteolytic activation of SREBPs and by enhancing degradation of HMG-CoA reductase. Here, we created Insig-double-knockout (Insig-DKO) mice that are homozygous for null mutations in Insig-1 and Insig-2. After 18.5 days of development, 96% of Insig-DKO embryos had defects in midline facial development, ranging from cleft palate (52%) to complete cleft face (44%). Middle and inner ear structures were abnormal, but teeth and skeletons were normal. The animals were lethargic and runted; they died within 1 day of birth. The livers and heads of Insig-DKO embryos overproduced sterols, causing a marked buildup of sterol intermediates. Treatment of pregnant mice with the HMG-CoA reductase inhibitor lovastatin reduced sterol synthesis in Insig-DKO embryos and reduced the pre-cholesterol intermediates. This treatment ameliorated the clefting syndrome so that 54% of Insig-DKO mice had normal faces, and only 7% had cleft faces. We conclude that buildup of pre-cholesterol sterol intermediates interferes with midline fusion of facial structures in mice. These findings have implications for the pathogenesis of the cleft palate component of Smith-Lemli-Opitz syndrome and other human malformation syndromes in which mutations in enzymes catalyzing steps in cholesterol biosynthesis produce a buildup of sterol intermediates.

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Year:  2006        PMID: 16955138      PMCID: PMC1555642          DOI: 10.1172/JCI28988

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  46 in total

1.  Generation of viable cholesterol-free mice.

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Journal:  Science       Date:  2003-12-19       Impact factor: 47.728

Review 2.  The Smith-Lemli-Opitz syndrome.

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Journal:  J Med Genet       Date:  2000-05       Impact factor: 6.318

3.  Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com.

Authors:  J M Derry; E Gormally; G D Means; W Zhao; A Meindl; R I Kelley; Y Boyd; G E Herman
Journal:  Nat Genet       Date:  1999-07       Impact factor: 38.330

4.  The gene mutated in bare patches and striated mice encodes a novel 3beta-hydroxysteroid dehydrogenase.

Authors:  X Y Liu; A W Dangel; R I Kelley; W Zhao; P Denny; M Botcherby; B Cattanach; J Peters; P R Hunsicker; A M Mallon; M A Strivens; R Bate; W Miller; M Rhodes; S D Brown; G E Herman
Journal:  Nat Genet       Date:  1999-06       Impact factor: 38.330

5.  Dual roles for cholesterol in mammalian cells.

Authors:  Fang Xu; Scott D Rychnovsky; Jitendra D Belani; Helen H Hobbs; Jonathan C Cohen; Robert B Rawson
Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-30       Impact factor: 11.205

Review 6.  RSH/Smith-Lemli-Opitz syndrome: a multiple congenital anomaly/mental retardation syndrome due to an inborn error of cholesterol biosynthesis.

Authors:  F D Porter
Journal:  Mol Genet Metab       Date:  2000 Sep-Oct       Impact factor: 4.797

7.  Simvastatin. A new therapeutic approach for Smith-Lemli-Opitz syndrome.

Authors:  P E Jira; R A Wevers; J de Jong; E Rubio-Gozalbo; F S Janssen-Zijlstra; A F van Heyst; R C Sengers; J A Smeitink
Journal:  J Lipid Res       Date:  2000-08       Impact factor: 5.922

8.  Markedly increased tissue concentrations of 7-dehydrocholesterol combined with low levels of cholesterol are characteristic of the Smith-Lemli-Opitz syndrome.

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Journal:  J Lipid Res       Date:  1995-01       Impact factor: 5.922

9.  Cholesterol supplementation does not improve developmental progress in Smith-Lemli-Opitz syndrome.

Authors:  Darryn M Sikora; Mark Ruggiero; Kersti Petit-Kekel; Louise S Merkens; William E Connor; Robert D Steiner
Journal:  J Pediatr       Date:  2004-06       Impact factor: 4.406

10.  Sterols regulate processing of carbohydrate chains of wild-type SREBP cleavage-activating protein (SCAP), but not sterol-resistant mutants Y298C or D443N.

Authors:  A Nohturfft; M S Brown; J L Goldstein
Journal:  Proc Natl Acad Sci U S A       Date:  1998-10-27       Impact factor: 11.205

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  35 in total

1.  β-Carotene and its cleavage enzyme β-carotene-15,15'-oxygenase (CMOI) affect retinoid metabolism in developing tissues.

Authors:  Youn-Kyung Kim; Lesley Wassef; Stacey Chung; Hongfeng Jiang; Adrian Wyss; William S Blaner; Loredana Quadro
Journal:  FASEB J       Date:  2011-02-01       Impact factor: 5.191

2.  Multiple malformations: a possible Sonic hedgehog phenotype?

Authors:  Helen Wainwright; Peter Beighton
Journal:  Virchows Arch       Date:  2009-02-10       Impact factor: 4.064

3.  Disruption of Dhcr7 and Insig1/2 in cholesterol metabolism causes defects in bone formation and homeostasis through primary cilium formation.

Authors:  Akiko Suzuki; Kenichi Ogata; Hiroki Yoshioka; Junbo Shim; Christopher A Wassif; Forbes D Porter; Junichi Iwata
Journal:  Bone Res       Date:  2020-01-02       Impact factor: 13.567

Review 4.  Developmental and extrahepatic physiological functions of SREBP pathway genes in mice.

Authors:  Luke J Engelking; Mary Jo Cantoria; Yanchao Xu; Guosheng Liang
Journal:  Semin Cell Dev Biol       Date:  2017-07-20       Impact factor: 7.727

Review 5.  SREBP-regulated lipid metabolism: convergent physiology - divergent pathophysiology.

Authors:  Hitoshi Shimano; Ryuichiro Sato
Journal:  Nat Rev Endocrinol       Date:  2017-08-29       Impact factor: 43.330

6.  Insig proteins mediate feedback inhibition of cholesterol synthesis in the intestine.

Authors:  Matthew R McFarlane; Guosheng Liang; Luke J Engelking
Journal:  J Biol Chem       Date:  2013-12-11       Impact factor: 5.157

7.  Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome.

Authors:  Keith W McLarren; Tesa M Severson; Christèle du Souich; David W Stockton; Lisa E Kratz; David Cunningham; Glenda Hendson; Ryan D Morin; Diane Wu; Jessica E Paul; Jianghong An; Tanya N Nelson; Athena Chou; Andrea E DeBarber; Louise S Merkens; Jacques L Michaud; Paula J Waters; Jingyi Yin; Barbara McGillivray; Michelle Demos; Guy A Rouleau; Karl-Heinz Grzeschik; Raffaella Smith; Patrick S Tarpey; Debbie Shears; Charles E Schwartz; Jozef Gecz; Michael R Stratton; Laura Arbour; Jane Hurlburt; Margot I Van Allen; Gail E Herman; Yongjun Zhao; Richard Moore; Richard I Kelley; Steven J M Jones; Robert D Steiner; F Lucy Raymond; Marco A Marra; Cornelius F Boerkoel
Journal:  Am J Hum Genet       Date:  2010-12-10       Impact factor: 11.025

8.  No evidence for mevalonate shunting in moderately affected children with Smith-Lemli-Opitz syndrome.

Authors:  Jean-Baptiste Roullet; Louise S Merkens; Anuradha S Pappu; Megan D Jacobs; Rolf Winter; William E Connor; Robert D Steiner
Journal:  J Inherit Metab Dis       Date:  2012-03-06       Impact factor: 4.982

9.  Identification of candidate downstream targets of TGFβ signaling during palate development by genome-wide transcript profiling.

Authors:  Richard C Pelikan; Junichi Iwata; Akiko Suzuki; Yang Chai; Joseph G Hacia
Journal:  J Cell Biochem       Date:  2013-04       Impact factor: 4.429

10.  Hair growth defects in Insig-deficient mice caused by cholesterol precursor accumulation and reversed by simvastatin.

Authors:  Bret M Evers; Midhat S Farooqi; John M Shelton; James A Richardson; Joseph L Goldstein; Michael S Brown; Guosheng Liang
Journal:  J Invest Dermatol       Date:  2010-01-21       Impact factor: 8.551

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