Evidence map›Paper›PMID 35781032›Full record

ArticleInsect biochemistry and molecular biology2022

Phenotypic analyses, protein localization, and bacteriostatic activity of Drosophila melanogaster transferrin-1.

Jacob J Weber, Lisa M Brummett, Michelle E Coca, Hiroko Tabunoki, Michael R Kanost, Emily J Ragan, Yoonseong Park, Maureen J Gorman

Open access · greenAbstract read
In one paragraph

Article in Insect biochemistry and molecular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 13 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Jacob J WeberDepartment of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, KS, 66506, USA. Electronic address: jjweber@ksu.edu.
Lisa M BrummettDepartment of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, KS, 66506, USA. Electronic address: lmbrumme@ksu.edu.
Michelle E CocaDepartment of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, KS, 66506, USA. Electronic address: mcmora@ksu.edu.
Hiroko TabunokiDepartment of Science of Biological Production, Graduate School of Agriculture, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu, Tokyo, 183-8509, Japan. Electronic address: h_tabuno@cc.tuat.ac.jp.
Michael R KanostDepartment of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, KS, 66506, USA. Electronic address: kanost@ksu.edu.
Emily J RaganDepartment of Chemistry and Biochemistry, Metropolitan State University of Denver, Denver, CO, 80217, USA. Electronic address: eragan@msudenver.edu.
Yoonseong ParkDepartment of Entomology, Kansas State University, Manhattan, KS, 66506, USA. Electronic address: ypark@ksu.edu.
Maureen J GormanDepartment of Biochemistry and Molecular Biophysics, Kansas State University, Manhattan, KS, 66506, USA. Electronic address: mgorman@ksu.edu.
Kansas State University · USMetropolitan State University of Denver · USTokyo University of Agriculture and Technology · JP

Funding

Resource Project CoreU41HG000739 · NHGRI · HARVARD UNIVERSITY · PI PERRIMON, NORBERT · 2014 to 2022
$32.3M
Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
DROSOPHILA GENOMICS RESOURCE CENTERP40OD010949 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Andrew Zelhof · 2012 to 2026
$9.4M
Supplement 2 to promote diversity in health related res.: protease systems in insR37GM041247 · NIGMS · KANSAS STATE UNIVERSITY · PI KANOST, MICHAEL R · 2011 to 2020
$3.8M
SERINE PROTEINASE INHIBITORS IN INSECTSR01GM041247 · NIGMS · KANSAS STATE UNIVERSITY · PI KANOST, MICHAEL R · 1994 to 2010
$3.1M
Function of hemolymph plasma proteins in insect immune responses (Equipment Supplement)R35GM141859 · NIGMS · KANSAS STATE UNIVERSITY · PI KANOST, MICHAEL R · 2021 to 2025
$2.0M
NHGRI NIH HHS U41 HG000739NIGMS NIH HHS R01 GM041247NIGMS NIH HHS R35 GM141859NIGMS NIH HHS R37 GM041247NIH HHS P40 OD010949NIH HHS P40 OD018537
6 · The paper itself

Abstract

Transferrin-1 (Tsf1) is an extracellular insect protein with a high affinity for iron. The functions of Tsf1 are still poorly understood; however, Drosophila melanogaster Tsf1 has been shown to influence iron distribution in the fly body and to protect flies against some infections. The goal of this study was to better understand the physiological functions of Tsf1 in D. melanogaster by 1) investigating Tsf1 null phenotypes, 2) determining tissue-specific localization of Tsf1, 3) measuring the concentration of Tsf1 in hemolymph, 4) testing Tsf1 for bacteriostatic activity, and 5) evaluating the effect of metal and paraquat treatments on Tsf1 abundance. Flies lacking Tsf1 had more iron than wild-type flies in specialized midgut cells that take up iron from the diet; however, the absence of Tsf1 had no effect on the iron content of whole midguts, fat body, hemolymph, or heads. Thus, as previous studies have suggested, Tsf1 appears to have a minor role in iron transport. Tsf1 was abundant in hemolymph from larvae (0.4 μM), pupae (1.4 μM), adult females (4.4 μM) and adult males (22 μM). Apo-Tsf1 at 1 μM had bacteriostatic activity whereas holo-Tsf1 did not, suggesting that Tsf1 can inhibit microbial growth by sequestering iron in hemolymph and other extracellular environments. This hypothesis was supported by detection of secreted Tsf1 in tracheae, testes and seminal vesicles. Colocalization of Tsf1 with an endosome marker in oocytes suggested that Tsf1 may provide iron to developing eggs; however, eggs from mothers lacking Tsf1 had the same amount of iron as control eggs, and they hatched at a wild-type rate. Thus, the primary function of Tsf1 uptake by oocytes may be to defend against infection rather than to provide eggs with iron. In beetles, Tsf1 plays a role in protection against oxidative stress. In contrast, we found that flies lacking Tsf1 had a typical life span and greater resistance to paraquat-induced oxidative stress. In addition, Tsf1 abundance remained unchanged in response to ingestion of iron, cadmium or paraquat or to injection of iron. These results suggest that Tsf1 has a limited role in protection against oxidative stress in D. melanogaster.

Indexed as

Drosophila melanogasterTransferrinAnimalsFemaleIronMaleOxidative StressParaquatPhenotypeIronParaquatTransferrinHemolymphImmunityInsectIronOxidative stressTransferrin

Identifiers

PMID35781032
PMCPMC9869689
OpenAlexW4283754605

What OpenQuestion holds

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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.