نتایج جستجو برای: seipin

تعداد نتایج: 156  

Journal: :Human molecular genetics 2014
Libin Zhou Jun Yin Conghui Wang Jiawei Liao George Liu Ling Chen

The Seipin gene was originally found to be responsible for type 2 congenital lipodystrophy and involved in lipid droplet formation. Seipin is highly expressed in the central nervous system as well. Seipin mutations have been identified in motor neuron diseases such as Silver syndrome and spastic paraplegia. In this study, we generated neuron-specific seipin knockout mice (seipin-nKO) to investi...

2014
Kenneth Wee Wulin Yang Shigeki Sugii Weiping Han

CGL (Congenital generalized lipodystrophy) is a genetic disorder characterized by near complete loss of adipose tissue along with increased ectopic fat storage in other organs including liver and muscle. Of the four CGL types, BSCL2 (Berardinelli-Seip Congenital lipodystrophy type 2), resulting from mutations in the BSCL2/seipin gene, exhibits the most severe lipodystrophic phenotype with loss ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Kimberly M Szymanski Derk Binns René Bartz Nick V Grishin Wei-Ping Li Anil K Agarwal Abhimanyu Garg Richard G W Anderson Joel M Goodman

Lipodystrophy is a disorder characterized by a loss of adipose tissue often accompanied by severe hypertriglyceridemia, insulin resistance, diabetes, and fatty liver. It can be inherited or acquired. The most severe inherited form is Berardinelli-Seip Congenital Lipodystrophy Type 2, associated with mutations in the BSCL2 gene. BSCL2 encodes seipin, the function of which has been entirely unkno...

2016
Martin Pagac Daniel E. Cooper Yanfei Qi Ivan E. Lukmantara Hoi Yin Mak Zengying Wu Yuan Tian Zhonghua Liu Mona Lei Ximing Du Charles Ferguson Damian Kotevski Pawel Sadowski Weiqin Chen Salome Boroda Thurl E. Harris George Liu Robert G. Parton Xun Huang Rosalind A. Coleman Hongyuan Yang

Berardinelli-Seip congenital lipodystrophy 2 (BSCL2) is caused by loss-of-function mutations in SEIPIN, a protein implicated in both adipogenesis and lipid droplet expansion but whose molecular function remains obscure. Here, we identify physical and functional interactions between SEIPIN and microsomal isoforms of glycerol-3-phosphate acyltransferase (GPAT) in multiple organisms. Compared to c...

Journal: :Human molecular genetics 2011
Xin Cui Yuhui Wang Yin Tang Yixiao Liu Liping Zhao Jingna Deng Guoheng Xu Xingui Peng Shenghong Ju George Liu Hongyuan Yang

Berardinelli-Seip congenital lipodystrophy type 2 (BSCL2) is an autosomal recessive disorder characterized by an almost complete loss of adipose tissue, insulin resistance and fatty liver. Here, we create the first murine model of BSCL2 by targeted disruption of seipin, the causative gene for BSCL2. Compared with their wild-type littermates, the seipin(-/-) mice are viable and of normal weight ...

2015
Md. Mesbah Uddin Talukder M.F. Michelle Sim Stephen O'Rahilly J. Michael Edwardson Justin J. Rochford

OBJECTIVE Disruption of the genes encoding either seipin or 1-acylglycerol-3-phosphate O-acyltransferase 2 (AGPAT2) causes severe congenital generalized lipodystrophy (CGL) in humans. However, the function of seipin in adipogenesis remains poorly defined. We demonstrated recently that seipin can bind the key adipogenic phosphatidic acid (PA) phosphatase lipin 1 and that seipin forms stable dode...

2015
Bethany R. Cartwright Derk D. Binns Christopher L. Hilton Sungwon Han Qiang Gao Joel M. Goodman

Seipin is necessary for both adipogenesis and lipid droplet (LD) organization in nonadipose tissues; however, its molecular function is incompletely understood. Phenotypes in the seipin-null mutant of Saccharomyces cerevisiae include aberrant droplet morphology (endoplasmic reticulum-droplet clusters and size heterogeneity) and sensitivity of droplet size to changes in phospholipid synthesis. I...

2016
Veijo T Salo Ilya Belevich Shiqian Li Leena Karhinen Helena Vihinen Corinne Vigouroux Jocelyne Magré Christoph Thiele Maarit Hölttä-Vuori Eija Jokitalo Elina Ikonen

Seipin is an endoplasmic reticulum (ER) membrane protein implicated in lipid droplet (LD) biogenesis and mutated in severe congenital lipodystrophy (BSCL2). Here, we show that seipin is stably associated with nascent ER-LD contacts in human cells, typically via one mobile focal point per LD Seipin appears critical for such contacts since ER-LD contacts were completely missing or morphologically...

Journal: :Human molecular genetics 2012
Daisuke Ito Takuya Yagi Masahito Ikawa Norihiro Suzuki

Gain-of-toxic mutations in the N-glycosylation motif of the seipin/BSCL2 gene (namely, the N88S and S90L mutations) cause autosomal dominant motor neuron diseases, termed 'seipinopathy'. Expressed mutant seipin is improperly folded and accumulates in the endoplasmic reticulum (ER), leading to an unfolded protein response (UPR). Furthermore, cells expressing mutant seipin contain unique cytoplas...

Journal: :Human molecular genetics 2013
Maarit Hölttä-Vuori Veijo T Salo Yuki Ohsaki Maximiliano L Suster Elina Ikonen

Mutations affecting the N-glycosylation site in Berardinelli-Seip lipodystrophy (BSCL)-associated gene BSCL2/seipin lead to a dominantly inherited spastic paraplegia termed seipinopathy. While the loss of function of seipin leads to severe congenital lipodystrophy, the effects of seipin N-glycosylation mutations on lipid balance in the nervous system are unknown. In this study, we show that exp...

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