Genetic variation of macronutrient tolerance in Drosophila melanogaster

被引:13
|
作者
Havula, E. [1 ,2 ,10 ]
Ghazanfar, S. [1 ,3 ]
Lamichane, N. [4 ,5 ]
Francis, D. [1 ]
Hasygar, K. [4 ,5 ]
Liu, Y. [4 ,5 ]
Alton, L. A. [6 ]
Johnstone, J. [6 ]
Needham, E. J. [1 ,2 ]
Pulpitel, T. [1 ]
Clark, T. [1 ]
Niranjan, H. N. [1 ]
Shang, V [1 ]
Tong, V [1 ]
Jiwnani, N. [1 ]
Audia, G. [1 ]
Alves, A. N. [6 ]
Sylow, L. [7 ,8 ]
Mirth, C. [6 ]
Neely, G. G. [1 ,2 ]
Yang, J. [1 ,9 ]
Hietakangas, V [4 ,5 ]
Simpson, S. J. [1 ,2 ]
Senior, A. M. [1 ,2 ,9 ]
机构
[1] Univ Sydney, Charles Perkins Ctr, Camperdown, NSW 2006, Australia
[2] Univ Sydney, Sch Life & Environm Sci, Camperdown, NSW 2006, Australia
[3] Univ Cambridge, Canc Res UK Cambridge Inst, Cambridge, England
[4] Univ Helsinki, Fac Biol & Environm Sci, Mol & Integrat Biosci Res Programme, Helsinki, Finland
[5] Univ Helsinki, Inst Biotechnol, Helsinki, Finland
[6] Monash Univ, Sch Biol Sci, Melbourne, Vic 3800, Australia
[7] Univ Copenhagen, Fac Sci, Dept Nutr Exercise & Sports, Sect Mol Physiol, Copenhagen, Denmark
[8] Univ Copenhagen, Fac Med & Hlth Sci, Dept Biomed Sci, DK-2200 Copenhagen, Denmark
[9] Univ Sydney, Sch Math & Stat, Camperdown, NSW 2006, Australia
[10] Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, Finland
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
DIET-INDUCED OBESITY; HIGH-FAT-DIET; IMPAIRED GLUCOSE-HOMEOSTASIS; INDUCED INSULIN-RESISTANCE; PROTEIN-KINASE; TOR PATHWAY; LIFE-SPAN; C57BL/6J; METABOLISM; MOUSE;
D O I
10.1038/s41467-022-29183-x
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
Carbohydrates, proteins and lipids are essential nutrients to all animals; however, closely related species, populations, and individuals can display dramatic variation in diet. Here we explore the variation in macronutrient tolerance in Drosophila melanogaster using the Drosophila genetic reference panel, a collection of similar to 200 strains derived from a single natural population. Our study demonstrates that D. melanogaster, often considered a "dietary generalist", displays marked genetic variation in survival on different diets, notably on high-sugar diet. Our genetic analysis and functional validation identify several regulators of macronutrient tolerance, including CG10960/GLUT8, Pkn and Eip75B. We also demonstrate a role for the JNK pathway in sugar tolerance and de novo lipogenesis. Finally, we report a role for tailless, a conserved orphan nuclear hormone receptor, in regulating sugar metabolism via insulin-like peptide secretion and sugar-responsive CCHamide-2 expression. Our study provides support for the use of nutrigenomics in the development of personalized nutrition.
引用
收藏
页数:16
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