Evidence map›Paper›PMID 24532012›Full record

ArticleParasitology research2014

Knockdown of APC/C-associated genes and its effect on viability and cell cycle of protozoan parasite of Trypanosoma brucei.

Mohamed Bessat

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Parasitology research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 86% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

1 author at 1 institution in 1 country.

Mohamed BessatDepartment of Parasitology, Faculty of Veterinary Medicine, Alexandria University, P.O. Box 22758, Edfina-Rasheed Line, Behaira, Egypt, mnooh2000@yahoo.com.
Alexandria University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the eukaryotic pathogen of Trypanosoma brucei, the anaphase promoting complex or cyclosome (APC/C) is composed of ten subunit proteins which are conserved in kinetoplastid protozoan parasites. During the course of APC/C characterization by PTP tagging and mass spectrometry, some other proteins were found to be associated in substoichiometric ratio to APC/C. These proteins could not be assigned as APC/C core components as they are below the threshold imposed by mass spectrometry identification and therefore they are termed non-core APC/C-associated proteins. Here in this study, functional roles of these proteins were investigated through reverse genetics approach. mRNAs of protein-encoding genes were individually knocked down by RNA interference and the resulting phenotypes were assayed through functional assays such as growth curve, cell cycle progression by flow cytometry, and DNA profiles by DAPI staining and microscopy examination. Based on the presented data, these proteins are playing essential functions in the cell biology of T. brucei; and more specifically, in regulating its cell cycle progression. Thus, the non-core APC/C-associated proteins appear to play important roles in complementing APC/C specialized function in the cell cycle of T. brucei.

Indexed as

Anaphase-Promoting Complex-CyclosomeCell CycleGene Knockdown TechniquesPhenotypeReverse GeneticsRNA InterferenceRNA, MessengerTrypanosoma brucei bruceiAnaphase-Promoting Complex-CyclosomeRNA, Messenger

Identifiers

PMID24532012
OpenAlexW2087197815

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.