Evidence map›Paper›PMID 37047677›Full record

ArticleInternational journal of molecular sciences2023

Bridging Gaps in HDR Improvement: The Role of MAD2L2, SCAI, and SCR7.

Arina A Anuchina, Milyausha I Zaynitdinova, Anna G Demchenko, Nadezhda A Evtushenko, Alexander V Lavrov, Svetlana A Smirnikhina

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

6 authors at 2 institutions in 1 country.

Arina A AnuchinaResearch Centre for Medical Genetics, Moskvorechie 1, 115522 Moscow, Russia.
Milyausha I ZaynitdinovaResearch Centre for Medical Genetics, Moskvorechie 1, 115522 Moscow, Russia.
Anna G DemchenkoResearch Centre for Medical Genetics, Moskvorechie 1, 115522 Moscow, Russia.ORCID 0000-0002-4460-7627
Nadezhda A EvtushenkoCenter for Precision Genome Editing and Genetic Technologies for Biomedicine, Pirogov Russian National Research Medical University, Ostrovityanova 1, 117997 Moscow, Russia.ORCID 0000-0003-1726-1939
Alexander V LavrovResearch Centre for Medical Genetics, Moskvorechie 1, 115522 Moscow, Russia.ORCID 0000-0003-4962-6947
Svetlana A SmirnikhinaResearch Centre for Medical Genetics, Moskvorechie 1, 115522 Moscow, Russia.
Research Centre for Medical Genetics · RUPirogov Russian National Research Medical University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to enhance homology-directed repair (HDR) efficiency in CRISPR/Cas-mediated genome editing by targeting three key factors regulating the balance between HDR and non-homologous end joining (NHEJ): MAD2L2, SCAI, and Ligase IV. In order to achieve this, a cellular model using mutated eGFP was designed to monitor HDR events. Results showed that MAD2L2 knockdown and SCR7 treatment significantly improved HDR efficiency during Cas9-mediated HDR repair of the mutated eGFP gene in the HEK293T cell line. Fusion protein Cas9-SCAI did not improve HDR. This study is the first to demonstrate that MAD2L2 knockdown during CRISPR-mediated gene editing in HEK293T cells can increase precise correction by up to 10.2 times. The study also confirmed a moderate but consistent effect of SCR7, an inhibitor of Ligase IV, which increased HDR by 1.7 times. These findings provide valuable insights into improving HDR-based genome editing efficiency.

Indexed as

CRISPR-Cas SystemsMad2 ProteinsRecombinational DNA RepairTranscription FactorsDNA End-Joining RepairGene EditingHEK293 CellsHumansLigasesLigasesMAD2L2 protein, humanMad2 ProteinsSCAI protein, humanTranscription FactorsCRISPR/CasHDRMAD2L2SCAISCR7

Identifiers

PMID37047677
PMCPMC10095018
OpenAlexW4362559633

What OpenQuestion holds

Textmetadata
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.