Evidence map›Paper›PMID 33693600›Full record

ArticleG3 (Bethesda, Md.)2021

An RNAi screen of the kinome in epithelial follicle cells of the Drosophila melanogaster ovary reveals genes required for proper germline death and clearance.

Diane P V Lebo, Alice Chirn, Jeffrey D Taylor, Andre Levan, Valentina Doerre Torres, Emily Agreda, Sandy B Serizier, Allison K Lord, Victoria K Jenkins, Kimberly McCall

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2021. 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
0.3field-weighted citation impact, top 47% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Expression of theJournal of neurogenetics · 2021
    Article
  5. Review
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

10 authors at 1 institution in 1 country.

Diane P V LeboDepartment of Biology, Boston University, Boston, MA 02215, USA.
Alice ChirnDepartment of Biology, Boston University, Boston, MA 02215, USA.
Jeffrey D TaylorDepartment of Biology, Boston University, Boston, MA 02215, USA.
Andre LevanDepartment of Biology, Boston University, Boston, MA 02215, USA.
Valentina Doerre TorresDepartment of Biology, Boston University, Boston, MA 02215, USA.
Emily AgredaDepartment of Biology, Boston University, Boston, MA 02215, USA.
Sandy B SerizierDepartment of Biology, Boston University, Boston, MA 02215, USA.
Allison K LordDepartment of Biology, Boston University, Boston, MA 02215, USA.
Victoria K JenkinsDepartment of Biology, Boston University, Boston, MA 02215, USA.
Kimberly McCallDepartment of Biology, Boston University, Boston, MA 02215, USA.
Boston University · US

Funding

Programmed Cell Death in Drosophila DevelopmentR01GM060574 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MCCALL, KIMBERLY A · 2001 to 2016
$4.5M
The coordination of cell death and corpse clearance in DrosophilaR35GM127338 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI Kimberly A McCall · 2018 to 2026
$4.1M
NIGMS NIH HHS R01 GM060574NIGMS NIH HHS R35 GM127338
6 · The paper itself

Abstract

Programmed cell death and cell corpse clearance are an essential part of organismal health and development. Cell corpses are often cleared away by professional phagocytes such as macrophages. However, in certain tissues, neighboring cells known as nonprofessional phagocytes can also carry out clearance functions. Here, we use the Drosophila melanogaster ovary to identify novel genes required for clearance by nonprofessional phagocytes. In the Drosophila ovary, germline cells can die at multiple time points. As death proceeds, the epithelial follicle cells act as phagocytes to facilitate the clearance of these cells. We performed an unbiased kinase screen to identify novel proteins and pathways involved in cell clearance during two death events. Of 224 genes examined, 18 demonstrated severe phenotypes during developmental death and clearance while 12 demonstrated severe phenotypes during starvation-induced cell death and clearance, representing a number of pathways not previously implicated in phagocytosis. Interestingly, it was found that several genes not only affected the clearance process in the phagocytes, but also non-autonomously affected the process by which germline cells died. This kinase screen has revealed new avenues for further exploration and investigation.

Indexed as

Drosophila melanogasterDrosophila ProteinsAnimalsApoptosisFemaleGerm CellsOvarian FollicleOvaryRNA InterferenceDrosophila Proteinscell deathDrosophilakinasephagocytosisphosphoinositide 3-kinase

Identifiers

PMID33693600
PMCPMC8022946
OpenAlexW3135567558

What OpenQuestion holds

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LicenceCC BY
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.