ArticleParasitology research2014
Knockdown of APC/C-associated genes and its effect on viability and cell cycle of protozoan parasite of Trypanosoma brucei.
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.
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.
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.
Who cites it
1 citing paper in PubMed, 2 citations in OpenAlex.
- Who Needs a Contractile Actomyosin Ring? The Plethora of Alternative Ways to Divide a Protozoan Parasite.Frontiers in cellular and infection microbiology · 2019Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
Registered trials
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.