The mevalonate pathway in C. elegans

被引:0
作者
Manish Rauthan
Marc Pilon
机构
[1] University of Gothenburg,Department of Cell and Molecular Biology
来源
Lipids in Health and Disease | / 10卷
关键词
mevalonate pathway; statin; coenzyme Q; dolichol; cholesterol; protein prenylation;
D O I
暂无
中图分类号
学科分类号
摘要
The mevalonate pathway in human is responsible for the synthesis of cholesterol and other important biomolecules such as coenzyme Q, dolichols and isoprenoids. These molecules are required in the cell for functions ranging from signaling to membrane integrity, protein prenylation and glycosylation, and energy homeostasis. The pathway consists of a main trunk followed by sub-branches that synthesize the different biomolecules. The majority of our knowledge about the mevalonate pathway is currently focused on the cholesterol synthesis branch, which is the target of the cholesterol-lowering statins; less is known about the function and regulation of the non-cholesterol-related branches. To study them, we need a biological system where it is possible to specifically modulate these metabolic branches individually or in groups. The nematode Caenorhabditis elegans (C. elegans) is a promising model to study these non-cholesterol branches since its mevalonate pathway seems very well conserved with that in human except that it has no cholesterol synthesis branch. The simple genetic makeup and tractability of C. elegans makes it relatively easy to identify and manipulate key genetic components of the mevalonate pathway, and to evaluate the consequences of tampering with their activity. This general experimental approach should lead to new insights into the physiological roles of the non-cholesterol part of the mevalonate pathway. This review will focus on the current knowledge related to the mevalonate pathway in C. elegans and its possible applications as a model organism to study the non-cholesterol functions of this pathway.
引用
收藏
相关论文
共 394 条
[1]  
Bentinger M(2010)Coenzyme Q--biosynthesis and functions Biochemical and biophysical research communications 396 74-79
[2]  
Tekle M(2005)Statins and cancer prevention Nat Rev Cancer 5 930-942
[3]  
Dallner G(2010)Overcoming multidrug-resistance in cancer: statins offer a logical candidate Medical hypotheses 74 237-239
[4]  
Demierre MF(2009)The use of statins in hematopoietic stem cell transplantation Current stem cell research & therapy 4 260-265
[5]  
Higgins PD(2010)3-Hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors in the treatment of central nervous system diseases Archives of neurology 67 1062-1067
[6]  
Gruber SB(2009)Statins inhibit protein lipidation and induce the unfolded protein response in the non-sterol producing nematode Proc Natl Acad Sci USA 106 18285-18290
[7]  
Hawk E(2011)Enzymes of the mevalonate pathway of isoprenoid biosynthesis Archives of biochemistry and biophysics 505 131-143
[8]  
Lippman SM(2005)Isopentenyl-diphosphate isomerase is essential for viability of Caenorhabditis elegans Molecular genetics and genomics: MGG 273 158-166
[9]  
Mehta NG(1994)Synthesis and function of isopentenyl adenosine derivatives in tRNA Biochimie 76 1152-1160
[10]  
Mehta M(2005)Translational operator of mRNA on the ribosome: how repressor proteins exclude ribosome binding Science 308 120-123