Evidence map›Paper›PMID 39169625›Full record

ArticlePlant communications2024

GENOMES UNCOUPLED PROTEIN1 binds to plastid RNAs and promotes their maturation.

Qian Tang, Duorong Xu, Benjamin Lenzen, Andreas Brachmann, Madhura M Yapa, Paymon Doroodian, Christian Schmitz-Linneweber, Tatsuru Masuda, Zhihua Hua, Dario Leister and 1 more

Abstract read
In one paragraph

Article in Plant communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

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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

11 authors.

Qian TangPlant Molecular Biology (Botany), Faculty of Biology, Ludwig-Maximilians-University München, 82152 Martinsried, Germany.
Duorong XuPlant Molecular Biology (Botany), Faculty of Biology, Ludwig-Maximilians-University München, 82152 Martinsried, Germany.
Benjamin LenzenMolecular Genetics, Humboldt-University Berlin, Philippstr. 13, 10115 Berlin, Germany.
Andreas BrachmannBiocenter of the LMU Munich, Genetics Section, Grosshaderner Str. 2-4, 82152 Planegg-Martinsried, Germany.
Madhura M YapaDepartment of Environmental and Plant Biology, Ohio University, Athens, OH 45701, USA.
Paymon DoroodianDepartment of Environmental and Plant Biology, Ohio University, Athens, OH 45701, USA.
Christian Schmitz-LinneweberMolecular Genetics, Humboldt-University Berlin, Philippstr. 13, 10115 Berlin, Germany.
Tatsuru MasudaGraduate School of Arts and Sciences, The University of Tokyo, Komaba, Meguro-ku 153-8902, Tokyo, Japan.
Zhihua HuaDepartment of Environmental and Plant Biology, Ohio University, Athens, OH 45701, USA.
Dario LeisterPlant Molecular Biology (Botany), Faculty of Biology, Ludwig-Maximilians-University München, 82152 Martinsried, Germany.
Tatjana KleinePlant Molecular Biology (Botany), Faculty of Biology, Ludwig-Maximilians-University München, 82152 Martinsried, Germany. Electronic address: tatjana.kleine@lmu.de.

Funding

Deutsche Forschungsgemeinschaft
6 · The paper itself

Abstract

Plastid biogenesis and the coordination of plastid and nuclear genome expression through anterograde and retrograde signaling are essential for plant development. GENOMES UNCOUPLED1 (GUN1) plays a central role in retrograde signaling during early plant development. The putative function of GUN1 has been extensively studied, but its molecular function remains controversial. Here, we evaluate published transcriptome data and generate our own data from gun1 mutants grown under signaling-relevant conditions to show that editing and splicing are not relevant for GUN1-dependent retrograde signaling. Our study of the plastid (post)transcriptome of gun1 seedlings with white and pale cotyledons demonstrates that GUN1 deficiency significantly alters the entire plastid transcriptome. By combining this result with a pentatricopeptide repeat code-based prediction and experimental validation by RNA immunoprecipitation experiments, we identified several putative targets of GUN1, including tRNAs and RNAs derived from ycf1.2, rpoC1, and rpoC2 and the ndhH-ndhA-ndhI-ndhG-ndhE-psaC-ndhD gene cluster. The absence of plastid rRNAs and the significant reduction of almost all plastid transcripts in white gun1 mutants account for the cotyledon phenotype. Our study provides evidence for RNA binding and maturation as the long-sought molecular function of GUN1 and resolves long-standing controversies. We anticipate that our findings will serve as a basis for subsequent studies on mechanisms of plastid gene expression and will help to elucidate the function of GUN1 in retrograde signaling.

Indexed as

ArabidopsisArabidopsis ProteinsPlastidsDNA-Binding ProteinsGene Expression Regulation, PlantRNA, PlantTranscriptomeArabidopsis ProteinsDNA-Binding ProteinsGUN1 protein, ArabidopsisRNA, PlantGUN1MORF2plastid (post)transcriptomeretrograde signalingRIP-seqRNA binding protein

Identifiers

PMID39169625
PMCPMC11671767

What Socratic 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 Socratic graph.