The Influence of Bacterial Diet on Fat Storage in C. elegans

被引:226
作者
Brooks, Kyleann K.
Liang, Bin
Watts, Jennifer L.
机构
[1] School of Molecular Biosciences, Washington State University, Pullman, WA
来源
PLOS ONE | 2009年 / 4卷 / 10期
关键词
CAENORHABDITIS-ELEGANS; ESCHERICHIA-COLI; REGULATES FAT; LIFE-SPAN; INSULIN; ACID; GENE; BIOSYNTHESIS; PATHWAY; MODEL;
D O I
10.1371/journal.pone.0007545
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: The nematode Caenorhabditis elegans has emerged as an important model for studies of the regulation of fat storage. C. elegans feed on bacteria, and various strains of E. coli are commonly used in research settings. However, it is not known whether particular bacterial diets affect fat storage and metabolism. Methodology/Principal Findings: Fat staining of fixed nematodes, as well as biochemical analysis of lipid classes, revealed considerable differences in fat stores in C. elegans growing on four different E. coli strains. Fatty acid composition and carbohydrate levels differ in the E. coli strains examined in these studies, however these nutrient differences did not appear to have a causative effect on fat storage levels in worms. Analysis of C. elegans strains carrying mutations disrupting neuroendocrine and other fat-regulatory pathways demonstrated that the intensity of Nile Red staining of live worms does not correlate well with biochemical methods of fat quantification. Several neuroendocrine pathway mutants and eating defective mutants show higher or lower fat storage levels than wild type, however, these mutants still show differences in fat stores when grown on different bacterial strains. Of all the mutants tested, only pept-1 mutants, which lack a functional intestinal peptide transporter, fail to show differential fat stores. Furthermore, fatty acid analysis of triacylglycerol stores reveals an inverse correlation between total fat stores and the levels of 15-methylpalmitic acid, derived from leucine catabolism. Conclusions: These studies demonstrate that nutritional cues perceived in the intestine regulate fat storage levels independently of neuroendocrine cues. The involvement of peptide transport and the accumulation of a fatty acid product derived from an amino acid suggest that specific peptides or amino acids may provide nutritional signals regulating fat metabolism and fat storage levels.
引用
收藏
页数:8
相关论文
共 47 条
[1]   Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes [J].
Ashrafi, K ;
Chang, FY ;
Watts, JL ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Ruvkun, G .
NATURE, 2003, 421 (6920) :268-272
[2]   Food transport in the C-elegans pharynx [J].
Avery, L ;
Shtonda, BB .
JOURNAL OF EXPERIMENTAL BIOLOGY, 2003, 206 (14) :2441-2457
[3]   A COMPLEMENTATION ANALYSIS OF RESTRICTION AND MODIFICATION OF DNA IN ESCHERICHIA COLI [J].
BOYER, HW ;
ROULLAND.D .
JOURNAL OF MOLECULAR BIOLOGY, 1969, 41 (03) :459-&
[4]   Assaying metabolic activity in ageing Caenorhabditis elegans [J].
Braeckman, BP ;
Houthoofd, K ;
De Vreese, A ;
Vanfleteren, JR .
MECHANISMS OF AGEING AND DEVELOPMENT, 2002, 123 (2-3) :105-119
[5]  
BRENNER S, 1974, GENETICS, V77, P71
[6]   Fatty acid desaturation and the regulation of adiposity in Caenorhabditis elegans [J].
Brock, Trisha J. ;
Browse, John ;
Watts, Jennifer L. .
GENETICS, 2007, 176 (02) :865-875
[7]   Tubby proteins: The plot thickens [J].
Carroll, K ;
Gomez, C ;
Shapiro, L .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (01) :55-63
[8]   Genetic uncoupling of the dsRNA-binding and RNA cleavage activities of the Escherichia coli endoribonuclease RNase III -: the effect of dsRNA binding on gene expression [J].
Dasgupta, S ;
Fernandez, L ;
Kameyama, L ;
Inada, T ;
Nakamura, Y ;
Pappas, A ;
Court, DL .
MOLECULAR MICROBIOLOGY, 1998, 28 (03) :629-640
[9]  
Davis MW, 1995, J NEUROSCI, V15, P8408
[10]   Neural and molecular dissection of a C. elegans sensory circuit that regulates fat and feeding [J].
Greer, Elisabeth R. ;
Perez, Carissa L. ;
Van Gilst, Marc R. ;
Lee, Brian H. ;
Ashrafi, Kaveh .
CELL METABOLISM, 2008, 8 (02) :118-131