Evidence map›Paper›PMID 37009824›Full record

ArticleEMBO reports2023

Rapid evolutionary repair by secondary perturbation of a primary disrupted transcriptional network.

Po-Chen Hsu, Yu-Hsuan Cheng, Chia-Wei Liao, Richard Ron R Litan, Yu-Ting Jhou, Florica Jean Ganaden Opoc, Ahmed A A Amine, Jun-Yi Leu

Open access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
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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

8 authors at 1 institution in 1 country.

Po-Chen HsuInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-9425-8154
Yu-Hsuan ChengInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0003-1624-2154
Chia-Wei LiaoInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-5256-3839
Richard Ron R LitanInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Yu-Ting JhouInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Florica Jean Ganaden OpocInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0002-3056-2309
Ahmed A A AmineInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Jun-Yi LeuInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.ORCID 0000-0001-5445-2799
Institute of Molecular Biology, Academia Sinica · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The discrete steps of transcriptional rewiring have been proposed to occur neutrally to ensure steady gene expression under stabilizing selection. A conflict-free switch of a regulon between regulators may require an immediate compensatory evolution to minimize deleterious effects. Here, we perform an evolutionary repair experiment on the Lachancea kluyveri yeast sef1Δ mutant using a suppressor development strategy. Complete loss of SEF1 forces cells to initiate a compensatory process for the pleiotropic defects arising from misexpression of TCA cycle genes. Using different selective conditions, we identify two adaptive loss-of-function mutations of IRA1 and AZF1. Subsequent analyses show that Azf1 is a weak transcriptional activator regulated by the Ras1-PKA pathway. Azf1 loss-of-function triggers extensive gene expression changes responsible for compensatory, beneficial, and trade-off phenotypes. The trade-offs can be alleviated by higher cell density. Our results not only indicate that secondary transcriptional perturbation provides rapid and adaptive mechanisms potentially stabilizing the initial stage of transcriptional rewiring but also suggest how genetic polymorphisms of pleiotropic mutations could be maintained in the population.

Indexed as

Gene Regulatory NetworksTranscription FactorsMutationPhenotypeSaccharomyces cerevisiaeTranscription FactorsAzf1compensatory evolutionLachancea kluyveriSef1trade-off

Identifiers

PMID37009824
PMCPMC10240213
OpenAlexW4362507330

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.