Evidence map›Paper›PMID 24558258›Full record

ArticleGenetics2014

Insight into insulin secretion from transcriptome and genetic analysis of insulin-producing cells of Drosophila.

Jian Cao, Julie Ni, Wenxiu Ma, Vanessa Shiu, Luis A Milla, Sangbin Park, Maria L Spletter, Sheng Tang, Jun Zhang, Xing Wei and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
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  5. Exploring the link between Parkinson's disease and type 2 diabetes mellitus in Drosophila.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  6. Article
  7. The Genetics of Diabetes: What We Can Learn fromInternational journal of molecular sciences · 2021
    Review
  8. Cell-type-specific, multicolor labeling of endogenous proteins with split fluorescent protein tags inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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  10. Article
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  12. Article
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  17. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Jian CaoDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, California 94305.
Julie Ni
Wenxiu Ma
Vanessa Shiu
Luis A Milla
Sangbin Park
Maria L Spletter
Sheng Tang
Jun Zhang
Xing Wei
Seung K Kim
Matthew P Scott
Stanford University · USHoward Hughes Medical Institute · US

Funding

TRAINING & OUTREACH COREP50GM107615 · NIGMS · STANFORD UNIVERSITY · PI SCOTT, MATTHEW P. · 2013 to 2017
$10.9M
Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Howard Hughes Medical InstituteNIGMS NIH HHS P50 GM107615NIGMS NIH HHS R01 GM084947NIGMS NIH HHS R01-GM084947
6 · The paper itself

Abstract

Insulin-producing cells (IPCs) in the Drosophila brain produce and release insulin-like peptides (ILPs) to the hemolymph. ILPs are crucial for growth and regulation of metabolic activity in flies, functions analogous to those of mammalian insulin and insulin-like growth factors (IGFs). To identify components functioning in IPCs to control ILP production, we employed genomic and candidate gene approaches. We used laser microdissection and messenger RNA sequencing to characterize the transcriptome of larval IPCs. IPCs highly express many genes homologous to genes active in insulin-producing β-cells of the mammalian pancreas. The genes in common encode ILPs and proteins that control insulin metabolism, storage, secretion, β-cell proliferation, and some not previously linked to insulin production or β-cell function. Among these novelties is unc-104, a kinesin 3 family gene, which is more highly expressed in IPCs compared to most other neurons. Knockdown of unc-104 in IPCs impaired ILP secretion and reduced peripheral insulin signaling. Unc-104 appears to transport ILPs along axons. As a complementary approach, we tested dominant-negative Rab genes to find Rab proteins required in IPCs for ILP production or secretion. Rab1 was identified as crucial for ILP trafficking in IPCs. Inhibition of Rab1 in IPCs increased circulating sugar levels, delayed development, and lowered weight and body size. Immunofluorescence labeling of Rab1 showed its tight association with ILP2 in the Golgi of IPCs. Unc-104 and Rab1 join other proteins required for ILP transport in IPCs.

Indexed as

Gene Expression ProfilingAnimalsAxonsCarbohydrate MetabolismConserved SequenceDrosophila melanogasterDrosophila ProteinsHemolymphInsulinInsulin-Secreting CellsInsulin SecretionLarvaMaleRNA, MessengerDrosophila ProteinsInsulinRNA, MessengerDrosophilaERGolgiinsulinkinesinlaser microdissectionpancreasRab1RNA-seqtransportUnc-104

Identifiers

PMID24558258
PMCPMC4012477
OpenAlexW2162653216

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.