Disruption of insulin pathways alters trehalose level and abolishes sexual dimorphism in locomotor activity in Drosophila

被引:83
作者
Belgacem, YH [1 ]
Martin, JR [1 ]
机构
[1] Univ Paris 11, CNRS, UMR 8620, NAMC,Equipe ATIPE Bases Neurales Mouvement Chez D, F-91405 Orsay, France
来源
JOURNAL OF NEUROBIOLOGY | 2006年 / 66卷 / 01期
关键词
fat body; insulin producing cells; insulin receptor; sexual dimorphism; trehalose level;
D O I
10.1002/neu.20193
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Insulin signaling pathways are implicated in several physiological processes in invertebrates, including the control of growth and life span; the latter of these has also been correlated with juvenile hormone (JH) deficiency. In turn, JH levels have been correlated with sex-specific differences in locomotor activity. Here, the involvement of the insulin signaling pathway in sex-specific differences in locomotor activity was investigated in Drosophila. Ablation of insulin-producing neurons in the adult pars-intercerebralis was found to increase trehalosemia and to abolish sexual dimorphism relevant to locomotion. Conversely, hyper-insulinemia induced by insulin injection or by over-expression of an insulin-like peptide decreases trehalosemia but does not affect locomotive behavior. Moreover, we also show that in the head of adult flies, the insulin receptor (InR) is expressed only in the fat body surrounding the brain. While both male and female InR mutants are hyper-trehalosemic, they exhibit similar patterns of locomotor activity. Our results indicate that first, insulin controls trehalosemia in adults, and second, like JH, it controls sex-specific differences in the locomotor activity of adult Drosophila in a manner independent of its effect on trehalose metabolism. (C) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:19 / 32
页数:14
相关论文
共 40 条
[1]   Neuroendocrine control of a sexually dimorphic behavior by a few neurons of the pars intercerebralis in Drosophila [J].
Belgacem, YH ;
Martin, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (23) :15154-15158
[2]   Drosophila's insulin/P13-kinase pathway coordinates cellular metabolism with nutritional conditions [J].
Britton, JS ;
Lockwood, WK ;
Li, L ;
Cohen, SM ;
Edgar, BA .
DEVELOPMENTAL CELL, 2002, 2 (02) :239-249
[3]   An evolutionarily conserved function of the Drosophila insulin receptor and insulin-like peptides in growth control [J].
Brogiolo, W ;
Stocker, H ;
Ikeya, T ;
Rintelen, F ;
Fernandez, R ;
Hafen, E .
CURRENT BIOLOGY, 2001, 11 (04) :213-221
[4]   Longer lifespan, altered metabolism, and stress resistance in Drosophila from ablation of cells making insulin-like ligands [J].
Broughton, SJ ;
Piper, MDW ;
Ikeya, T ;
Bass, TM ;
Jacobson, J ;
Driege, Y ;
Martinez, P ;
Hafen, E ;
Withers, DJ ;
Leevers, SJ ;
Partridge, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (08) :3105-3110
[5]   Localization of an insulin-like peptide in brains of two flies [J].
Cao, C ;
Brown, MR .
CELL AND TISSUE RESEARCH, 2001, 304 (02) :317-321
[6]   The Drosophila insulin receptor is required for normal growth [J].
Chen, C ;
Jack, J ;
Garofalo, RS .
ENDOCRINOLOGY, 1996, 137 (03) :846-856
[7]   Role of trehalose phosphate synthase in anoxia tolerance and development in Drosophila melanogaster [J].
Chen, QF ;
Ma, E ;
Behar, KL ;
Xu, T ;
Haddad, GG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (05) :3274-3279
[8]   Extension of life-span by loss of CHICO, a Drosophila insulin receptor substrate protein [J].
Clancy, DJ ;
Gems, D ;
Harshman, LG ;
Oldham, S ;
Stocker, H ;
Hafen, E ;
Leevers, SJ ;
Partridge, L .
SCIENCE, 2001, 292 (5514) :104-106
[9]   The Drosophila takeout gene is regulated by the somatic sex-determination pathway and affects male courtship behavior [J].
Dauwalder, B ;
Tsujimoto, S ;
Moss, J ;
Mattox, W .
GENES & DEVELOPMENT, 2002, 16 (22) :2879-2892
[10]   HMG-COA REDUCTASE INHIBITOR FLUVASTATIN INHIBITS INSECT JUVENILE-HORMONE BIOSYNTHESIS [J].
DEBERNARD, S ;
ROSSIGNOL, F ;
COUILLAUD, F .
GENERAL AND COMPARATIVE ENDOCRINOLOGY, 1994, 95 (01) :92-98