Evidence map›Paper›PMID 28918480›Full record

ArticleCurrent genetics2018

Sgs1 helicase is required for efficient PCNA monoubiquitination and translesion DNA synthesis in Saccharomyces cerevisiae.

Fangfang Li, Lindsay G Ball, Li Fan, Michelle Hanna, Wei Xiao

Abstract read
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In one paragraph

Article in Current genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 12 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

5 authors at 3 institutions in 2 countries.

Fangfang LiBeijing Key Laboratory of DNA Damage Responses and College of Life Sciences, Capital Normal University, Beijing, 100048, China.
Lindsay G BallDepartment of Microbiology and Immunology, University of Saskatchewan, Saskatoon, SK, S7N 5E5, Canada.
Li FanBeijing Key Laboratory of DNA Damage Responses and College of Life Sciences, Capital Normal University, Beijing, 100048, China.
Michelle HannaDepartment of Microbiology and Immunology, University of Saskatchewan, Saskatoon, SK, S7N 5E5, Canada.
Wei XiaoBeijing Key Laboratory of DNA Damage Responses and College of Life Sciences, Capital Normal University, Beijing, 100048, China. wei.xiao@usask.ca.ORCID http://orcid.org/0000-0001-7568-0782
Capital Normal University · CNUniversity of Saskatchewan · CABeijing Normal University · CN

Funding

National Natural Science Foundation of China 31670068
6 · The paper itself

Abstract

DNA-damage tolerance (DDT) is employed by eukaryotes to deal with replication blocks on the template strand, and is divided into two parallel pathways that are activated by sequential ubiquitination of proliferating cell nuclear antigen (PCNA) at the Lys164 residue. Rad6-Rad18-mediated PCNA monoubiquitination promotes translesion DNA synthesis (TLS) and the monoubiquitinated PCNA can be further polyubiquitinated by an Mms2-Ubc13-Rad5 complex, leading to error-free lesion bypass. We previously reported that the DNA helicase Sgs1 is required for error-free lesion bypass, probably through the double-Holliday junction migration and subsequent resolution. Surprisingly, a synthetic genetic array (SGA) screen using rev1 and rev3 as baits did not reveal an anticipated synthetic effect with sgs1, indicating a possible involvement of Sgs1 in TLS. Here, we report detailed genetic analyses demonstrating that Sgs1 plays a key role in efficient TLS and that it is probably required for the signaling of DNA damage leading to PCNA monoubiquitination. These studies collectively illustrate that Sgs1 participates in both branches of DDT and possibly plays a role in pathway choice.

Indexed as

DNADNA-Binding ProteinsDNA DamageDNA-Directed DNA PolymeraseDNA HelicasesMultiprotein ComplexesNucleotidyltransferasesProliferating Cell Nuclear AntigenRecQ HelicasesSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsUbiquitinationUbiquitin-Conjugating EnzymesUbiquitin-Protein LigasesY-Family DNA PolymerasesDNADNA-Binding ProteinsDNA-Directed DNA PolymeraseDNA HelicasesMMS2 protein, S cerevisiaeMultiprotein ComplexesNucleotidyltransferasesProliferating Cell Nuclear AntigenRAD18 protein, S cerevisiaeRAD5 protein, S cerevisiaeRAD6 protein, S cerevisiaeRecQ HelicasesREV1 protein, S cerevisiaeREV3 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsSGS1 protein, S cerevisiaeUBC13 protein, S cerevisiaeUbiquitin-Conjugating EnzymesUbiquitin-Protein LigasesY-Family DNA PolymerasesDNA-damage toleranceEpistasisSaccharomyces cerevisiaeSgs1Translesion DNA synthesis

Identifiers

PMID28918480
OpenAlexW2755150594

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.