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Insulin Signaling Couples Growth and Early Maturation to Cholesterol Intake

https://doi.org/10.1101/2021.06.07.447368

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Metabolism and growth adaptation to environmental conditions in Drosophila

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Peptidergic paracrine and endocrine cells in the midgut of the fruit fly maggot

inferredcites →https://doi.org/10.1007/s10545-014-9794-4openalex-snapshot

Complex lipid trafficking in Niemann‐Pick disease type C

inferredcites →https://doi.org/10.1007/s11154-007-9028-2openalex-snapshot

Neuroendocrine factors in the initiation of puberty: The emergent role of kisspeptin

inferredcites →https://doi.org/10.1016/j.celrep.2012.09.011openalex-snapshot

A GAL4-Driver Line Resource for Drosophila Neurobiology

inferredcites →https://doi.org/10.1016/j.cmet.2007.01.011openalex-snapshot

Drosophila NPC1b Promotes an Early Step in Sterol Absorption from the Midgut Epithelium

inferredcites →https://doi.org/10.1016/j.cmet.2009.08.002openalex-snapshot

Remote Control of Insulin Secretion by Fat Cells in Drosophila

inferredcites →https://doi.org/10.1016/j.cois.2020.10.005openalex-snapshot

Interorgan communication in the control of metamorphosis

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Ras Activity in the Drosophila Prothoracic Gland Regulates Body Size and Developmental Rate via Ecdysone Release

inferredcites →https://doi.org/10.1016/j.cub.2005.09.017openalex-snapshot

The Role of the Prothoracic Gland in Determining Critical Weight for Metamorphosis in Drosophila melanogaster

inferredcites →https://doi.org/10.1016/j.cub.2013.01.072openalex-snapshot

bantam miRNA Promotes Systemic Growth by Connecting Insulin Signaling and Ecdysone Production

inferredcites →https://doi.org/10.1016/j.cub.2017.04.048openalex-snapshot

Warts Signaling Controls Organ and Body Growth through Regulation of Ecdysone

inferredcites →https://doi.org/10.1016/j.cub.2019.01.053openalex-snapshot

AstA Signaling Functions as an Evolutionary Conserved Mechanism Timing Juvenile to Adult Transition

inferredcites →https://doi.org/10.1016/j.cub.2019.07.027openalex-snapshot

A Tissue- and Temporal-Specific Autophagic Switch Controls Drosophila Pre-metamorphic Nutritional Checkpoints

inferredcites →https://doi.org/10.1016/j.cub.2020.03.050openalex-snapshot

The Corazonin-PTTH Neuronal Axis Controls Systemic Body Growth by Regulating Basal Ecdysteroid Biosynthesis in Drosophila melanogaster

inferredcites →https://doi.org/10.1016/j.cub.2021.01.080openalex-snapshot

The Upd3 cytokine couples inflammation to maturation defects in Drosophila

inferredcites →https://doi.org/10.1016/j.devcel.2007.11.003openalex-snapshot

Prothoracicotropic Hormone Regulates Developmental Timing and Body Size in Drosophila

inferredcites →https://doi.org/10.1016/j.devcel.2008.08.003openalex-snapshot

The TOR Pathway Couples Nutrition and Developmental Timing in Drosophila

inferredcites →https://doi.org/10.1016/j.devcel.2009.10.008openalex-snapshot

A Fat Body-Derived IGF-like Peptide Regulates Postfeeding Growth in Drosophila

inferredcites →https://doi.org/10.1016/j.devcel.2009.10.009openalex-snapshot

A Drosophila Insulin-like Peptide Promotes Growth during Nonfeeding States

inferredcites →https://doi.org/10.1016/j.devcel.2015.10.003openalex-snapshot

Signaling from Glia and Cholinergic Neurons Controls Nutrient-Dependent Production of an Insulin-like Peptide for Drosophila Body Growth

inferredcites →https://doi.org/10.1016/j.devcel.2016.05.015openalex-snapshot

A Drosophila Genome-Wide Screen Identifies Regulators of Steroid Hormone Production and Developmental Timing

inferredcites →https://doi.org/10.1016/j.devcel.2019.01.007openalex-snapshot

Autophagy-Mediated Cholesterol Trafficking Controls Steroid Production

inferredcites →https://doi.org/10.1016/j.tem.2009.02.004openalex-snapshot

Childhood obesity and the timing of puberty

inferredcites →https://doi.org/10.1016/j.tem.2011.09.002openalex-snapshot

Leptin action in pubertal development: recent advances and unanswered questions

inferredcites →https://doi.org/10.1016/j.ydbio.2006.07.023openalex-snapshot

Spook and Spookier code for stage-specific components of the ecdysone biosynthetic pathway in Diptera

inferredcites →https://doi.org/10.1016/j.ydbio.2019.09.009openalex-snapshot

Hedgehog signaling promotes lipolysis in adipose tissue through directly regulating Bmm/ATGL lipase

inferredcites →https://doi.org/10.1016/s0022-2275(20)37830-5openalex-snapshot

Adipose tissue and cholesterol metabolism.

inferredcites →https://doi.org/10.1016/s0092-8674(03)00713-xopenalex-snapshot

A Nutrient Sensor Mechanism Controls Drosophila Growth

inferredcites →https://doi.org/10.1016/s0960-9822(02)01043-6openalex-snapshot

Nutrient-Dependent Expression of Insulin-like Peptides from Neuroendocrine Cells in the CNS Contributes to Growth Regulation in Drosophila

inferredcites →https://doi.org/10.1038/ncomms10083openalex-snapshot

Cold-sensing regulates Drosophila growth through insulin-producing cells

inferredcites →https://doi.org/10.1038/ng.301openalex-snapshot

Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations

inferredcites →https://doi.org/10.1073/pnas.1506638112openalex-snapshot

Correction for Sano et al., Two distinct signaling pathways in hair cycle induction: Stat3-dependent and -independent pathways

inferredcites →https://doi.org/10.1073/pnas.96.4.1657openalex-snapshot

Localization of Niemann–Pick C1 protein in astrocytes: Implications for neuronal degeneration in Niemann– Pick type C disease

inferredcites →https://doi.org/10.1080/15548627.2019.1617608openalex-snapshot

Autophagy regulates steroid production by mediating cholesterol trafficking in endocrine cells

inferredcites →https://doi.org/10.1093/benz/9780199773787.article.b00181317openalex-snapshot

Texada, Moreno

inferredcites →https://doi.org/10.1101/gad.249763.114openalex-snapshot

Production of systemically circulating Hedgehog by the intestine couples nutrition to growth and development

inferredcites →https://doi.org/10.1126/science.1070058openalex-snapshot

Ablation of Insulin-Producing Neurons in Flies: Growth and Diabetic Phenotypes

inferredcites →https://doi.org/10.1126/science.1119432openalex-snapshot

Antagonistic Actions of Ecdysone and Insulins Determine Final Size in Drosophila

inferredcites →https://doi.org/10.1126/science.1176450openalex-snapshot

The Insect Neuropeptide PTTH Activates Receptor Tyrosine Kinase Torso to Initiate Metamorphosis

inferredcites →https://doi.org/10.1126/science.1216689openalex-snapshot

Secreted Peptide Dilp8 Coordinates Drosophila Tissue Growth with Developmental Timing

inferredcites →https://doi.org/10.1126/science.1216735openalex-snapshot

Imaginal Discs Secrete Insulin-Like Peptide 8 to Mediate Plasticity of Growth and Maturation

inferredcites →https://doi.org/10.1126/science.1241210openalex-snapshot

Neuroendocrine Control of Drosophila Larval Light Preference

inferredcites →https://doi.org/10.1126/science.aag1417openalex-snapshot

Lysosomal cholesterol activates mTORC1 via an SLC38A9–Niemann-Pick C1 signaling complex

inferredcites →https://doi.org/10.1152/physiolgenomics.00006.2015openalex-snapshot

Extreme obesity is associated with variation in genes related to the circadian rhythm of food intake and hypothalamic signaling

inferredcites →https://doi.org/10.1158/0008-5472.can-15-2613openalex-snapshot

The Role of Cholesterol in Cancer

inferredcites →https://doi.org/10.1161/atvbaha.110.207191openalex-snapshot

Niemann-Pick C1 Modulates Hepatic Triglyceride Metabolism and Its Genetic Variation Contributes to Serum Triglyceride Levels

inferredcites →https://doi.org/10.1186/1472-6823-13-5openalex-snapshot

NPC1 in human white adipose tissue and obesity

inferredcites →https://doi.org/10.1186/1741-7015-10-140openalex-snapshot

Mammalian NPC1 genes may undergo positive selection and human polymorphisms associate with type 2 diabetes

inferredcites →https://doi.org/10.1210/er.2010-0013openalex-snapshot

The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders

inferredcites →https://doi.org/10.1242/dev.044560openalex-snapshot

Survival strategies of a sterol auxotroph

inferredcites →https://doi.org/10.1242/dev.099739openalex-snapshot

Dynamic feedback circuits function as a switch for shaping a maturation-inducing steroid pulse in Drosophila

inferredcites →https://doi.org/10.1242/dev.188110openalex-snapshot

Ecdysone-dependent feedback regulation of prothoracicotropic hormone controls the timing of developmental maturation

inferredcites →https://doi.org/10.1242/jcs.120261openalex-snapshot

The IGFBP7 homolog Imp-L2 promotes insulin signaling in distinct neurons of the Drosophila brain

inferredcites →https://doi.org/10.1371/journal.pbio.0030289openalex-snapshot

The Temporal Requirements for Insulin Signaling During Development in Drosophila

inferredcites →https://doi.org/10.1371/journal.pbio.2006749openalex-snapshot

Avoidance response to CO2 in the lateral horn

inferredcites →https://doi.org/10.1371/journal.pbio.3000609openalex-snapshot

Snail synchronizes endocycling in a TOR-dependent manner to coordinate entry and escape from endoreplication pausing during the Drosophila critical weight checkpoint

inferredcites →https://doi.org/10.1371/journal.pgen.1002828openalex-snapshot

Lipoproteins in Drosophila melanogaster—Assembly, Function, and Influence on Tissue Lipid Composition

inferredcites →https://doi.org/10.1371/journal.pgen.1004555openalex-snapshot

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

inferredcites →https://doi.org/10.1371/journal.pgen.1006583openalex-snapshot

Nutrient-Dependent Endocycling in Steroidogenic Tissue Dictates Timing of Metamorphosis in Drosophila melanogaster

inferredcites →https://doi.org/10.1371/journal.pone.0005072openalex-snapshot

Increased Insulin/Insulin Growth Factor Signaling Advances the Onset of Metamorphosis in Drosophila

inferredcites →https://doi.org/10.1371/journal.pone.0146758openalex-snapshot

Effects of Synthetic Diets Enriched in Specific Nutrients on Drosophila Development, Body Fat, and Lifespan

inferredcites →https://doi.org/10.1523/jneurosci.4367-07.2008openalex-snapshot

Organization and Function of the Blood–Brain Barrier in Drosophila

inferredcites →https://doi.org/10.1523/jneurosci.5529-07.2008openalex-snapshot

Neuronal Loss of Drosophila NPC1a Causes Cholesterol Aggregation and Age-Progressive Neurodegeneration

inferredcites →https://doi.org/10.1534/genetics.120.303095openalex-snapshot

Regulation of Body Size and Growth Control

inferredcites →https://doi.org/10.1542/peds.2007-1813fopenalex-snapshot

Link Between Body Fat and the Timing of Puberty

inferredcites →https://doi.org/10.2337/db16-0877openalex-snapshot

Rare Loss-of-Function Variants in NPC1 Predispose to Human Obesity

inferredcites →https://doi.org/10.3109/01677063.2011.642910openalex-snapshot

Mapping Neural Circuits with Activity-Dependent Nuclear Import of a Transcription Factor

inferredcites →https://doi.org/10.5194/acp-2016-268-rc1openalex-snapshot

Review of Christensen et al. (2016)

inferredcites →https://doi.org/10.7554/elife.02862openalex-snapshot

Delivery of circulating lipoproteins to specific neurons in the Drosophila brain regulates systemic insulin signaling

inferredcites →https://doi.org/10.7554/elife.03091openalex-snapshot

Nutritional control of body size through FoxO-Ultraspiracle mediated ecdysone biosynthesis

inferredcites →https://doi.org/10.7554/elife.03091.023openalex-snapshot

Author response: Nutritional control of body size through FoxO-Ultraspiracle mediated ecdysone biosynthesis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1016/j.aqrep.2024.102297openalex-snapshot

Exploring the effects of dietary cholesterol on growth, immunity, and lipid metabolism of juvenile Chinese mitten crabs (Eriocheir sinensis)

inferred← citeshttps://doi.org/10.1101/2023.08.15.553340openalex-snapshot

A neuronal relay mediates muscle-adipose communication that drives systemic metabolic adaptation to high-sugar diets

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