A Genetic Strategy to Measure Circulating Drosophila Insulin Reveals Genes Regulating Insulin Production and Secretion

被引:132
作者
Park, Sangbin [1 ]
Alfa, Ronald W. [1 ,2 ]
Topper, Sydni M. [1 ]
Kim, Grace E. S. [1 ]
Kockel, Lutz [1 ]
Kim, Seung K. [1 ,3 ,4 ]
机构
[1] Stanford Univ, Dept Dev Biol, Sch Med, Stanford, CA 94305 USA
[2] Stanford Univ, Neurosci Program, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Med, Sch Med, Div Oncol, Stanford, CA 94305 USA
[4] Stanford Univ, Howard Hughes Med Inst, Sch Med, Stanford, CA 94305 USA
关键词
EXTENDS LIFE-SPAN; FLUORESCENT PROTEIN; RECEPTOR; GLUCOSE; CELLS; EXPRESSION; RESISTANCE; NEURONS; MICE; PEPTIDE;
D O I
10.1371/journal.pgen.1004555
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Insulin is a major regulator of metabolism in metazoans, including the fruit fly Drosophila melanogaster. Genome-wide association studies (GWAS) suggest a genetic basis for reductions of both insulin sensitivity and insulin secretion, phenotypes commonly observed in humans with type 2 diabetes mellitus (T2DM). To identify molecular functions of genes linked to T2DM risk, we developed a genetic tool to measure insulin-like peptide 2 (Ilp2) levels in Drosophila, a model organism with superb experimental genetics. Our system permitted sensitive quantification of circulating Ilp2, including measures of Ilp2 dynamics during fasting and re-feeding, and demonstration of adaptive Ilp2 secretion in response to insulin receptor haploinsufficiency. Tissue specific dissection of this reduced insulin signaling phenotype revealed a critical role for insulin signaling in specific peripheral tissues. Knockdown of the Drosophila orthologues of human T2DM risk genes, including GLIS3 and BCL11A, revealed roles of these Drosophila genes in Ilp2 production or secretion. Discovery of Drosophila mechanisms and regulators controlling in vivo insulin dynamics should accelerate functional dissection of diabetes genetics.
引用
收藏
页数:11
相关论文
共 42 条
[1]
Early neonatal death in mice homozygous for a null allele of the insulin receptor gene [J].
Accili, D ;
Drago, J ;
Lee, EJ ;
Johnson, MD ;
Cool, MH ;
Salvatore, P ;
Asico, LD ;
Jose, PA ;
Taylor, SI ;
Westphal, H .
NATURE GENETICS, 1996, 12 (01) :106-109
[2]
Drosophila insulin-like peptide-6 (dilp6) expression from fat body extends lifespan and represses secretion of Drosophila insulin-like peptide-2 from the brain [J].
Bai, Hua ;
Kang, Ping ;
Tatar, Marc .
AGING CELL, 2012, 11 (06) :978-985
[3]
THE EFFECT OF A 72-H FAST ON PLASMA-LEVELS OF PITUITARY, ADRENAL, THYROID, PANCREATIC AND GASTROINTESTINAL HORMONES IN HEALTHY-MEN AND WOMEN [J].
BEER, SF ;
BIRCHAM, PMM ;
BLOOM, SR ;
CLARK, PM ;
HALES, CN ;
HUGHES, CM ;
JONES, CT ;
MARSH, DR ;
RAGGATT, PR ;
FINDLAY, ALR .
JOURNAL OF ENDOCRINOLOGY, 1989, 120 (02) :337-350
[4]
From mice to men: Insights into the insulin resistance syndromes [J].
Biddinger, SB ;
Kahn, CR .
ANNUAL REVIEW OF PHYSIOLOGY, 2006, 68 :123-158
[5]
The genetics of type 2 diabetes: what have we learned from GWAS? [J].
Billings, Liana K. ;
Florez, Jose C. .
YEAR IN DIABETES AND OBESITY, 2010, 1212 :59-77
[6]
IMPAIRMENT OF THE PRIMING EFFECT OF GLUCOSE ON INSULIN-SECRETION FROM ISOLATED ISLETS OF AGING RATS [J].
BOMBARA, M ;
MASIELLO, P ;
NOVELLI, M ;
BERGAMINI, E .
ACTA DIABETOLOGICA, 1995, 32 (01) :69-73
[7]
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
[8]
A muscle-specific insulin receptor knockout exhibits features of the metabolic syndrome of NIDDM without altering glucose tolerance [J].
Bruning, JC ;
Michael, MD ;
Winnay, JN ;
Hayashi, T ;
Horsch, D ;
Accili, D ;
Goodyear, LJ ;
Kahn, CR .
MOLECULAR CELL, 1998, 2 (05) :559-569
[9]
Development of a novel polygenic model of NIDDM in mice heterozygous for IR and IRS-1 null alleles [J].
Bruning, JC ;
Winnay, J ;
BonnerWeir, S ;
Taylor, SI ;
Accili, D ;
Kahn, CR .
CELL, 1997, 88 (04) :561-572
[10]
Opposing effects of dietary protein and sugar regulate a transcriptional target of Drosophila insulin-like peptide signaling [J].
Buch, Susanne ;
Melcher, Christoph ;
Bauer, Matthias ;
Katzenberger, Joerg ;
Pankratz, Michael J. .
CELL METABOLISM, 2008, 7 (04) :321-332