Evidence map›Paper›PMID 38381201›Full record

ArticleFunctional & integrative genomics2024

OsCSN2 orchestrates Oryza sativa L. growth and development through modulation of the GA and BR pathways.

Shining Han, Weijie Yue, Anar Bao, Tongtong Jiao, Yanxi Liu, Hua Zeng, Kai Song, Ming Wu, Liquan Guo

Abstract read
PubMed Publisher
In one paragraph

Article in Functional & integrative genomics, 2024. 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
0.9field-weighted citation impact, top 28% 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. Article
  2. COP9 Signalosome's Role in Plant Defense Mechanisms.Plants (Basel, Switzerland) · 2025
    Review
  3. Article
  4. Effects of CSN1/CSN2 Mutants in Flavonoid Metabolism on Rice (International journal of molecular sciences · 2025
    Article
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

9 authors at 2 institutions in 1 country.

Shining HanCollege of Life Sciences, Jilin Agricultural University, Changchun, 130118, People's Republic of China.
Weijie YueCollege of Life Sciences, Jilin Agricultural University, Changchun, 130118, People's Republic of China.
Anar BaoCollege of Life Sciences, Jilin Agricultural University, Changchun, 130118, People's Republic of China.
Tongtong JiaoCollege of Life Sciences, Jilin Agricultural University, Changchun, 130118, People's Republic of China.
Yanxi LiuCollege of Life Sciences, Jilin Agricultural University, Changchun, 130118, People's Republic of China.
Hua ZengCollege of Life Sciences, Jilin Agricultural University, Changchun, 130118, People's Republic of China.
Kai SongSchool of Life Science, Changchun Normal University, Changchun, 130032, People's Republic of China.
Ming WuCollege of Life Sciences, Jilin Agricultural University, Changchun, 130118, People's Republic of China. mingw@jlau.edu.cn.
Liquan GuoCollege of Life Sciences, Jilin Agricultural University, Changchun, 130118, People's Republic of China. guolq948@nenu.edu.cn.
Jilin Agricultural University · CNChangchun Normal University · CN

Funding

Department of Science and Technology of Jilin Province 20220402060GHDepartment of Science and Technology of Jilin Province 20230402020GH
6 · The paper itself

Abstract

The COP9 signalosome (CSN) is a conserved protein complex found in higher eukaryotes, consisting of eight subunits, and it plays a crucial role in regulating various processes of plant growth and development. Among these subunits, CSN2 is one of the most conserved components within the COP9 signalosome complex. Despite its prior identification in other species, its specific function in Oryza sativa L. (Rice) has remained poorly understood. In this study, we investigated the role of CSN2 in rice using gene editing CRISPR/Cas9 technology and overexpression techniques. We created two types of mutants: the oscsn2 mutant and the OsCSN2-OE mutant, both in the background of rice, and also generated point mutants of OsCSN2 (OsCSN2K64E, OsCSN2K67E, OsCSN2K71E and OsCSN2K104E) to further explore the regulatory function of OsCSN2. Phenotypic observation and gene expression analysis were conducted on plants from the generated mutants, tracking their growth from the seedling to the heading stages. The results showed that the loss and modification of OsCSN2 had limited effects on plant growth and development during the early stages of both the wild-type and mutant plants. However, as the plants grew to 60 days, significant differences emerged. The OsCSN2 point mutants exhibited increased tillering compared to the OsCSN2-OE mutant plants, which were already at the tillering stage. On the other hand, the OsCSN2 point mutant had already progressed to the heading and flowering stages, with the shorter plants. These results, along with functional predictions of the OsCSN2 protein, indicated that changes in the 64th, 67th, 71st, and 104th amino acids of OsCSN2 affected its ubiquitination site, influencing the ubiquitination function of CSN and consequently impacting the degradation of the DELLA protein SLR1. Taken together, it can be speculated that OsCSN2 plays a key role in GA and BR pathways by influencing the functional regulation of the transcription factor SLR1 in CSN, thereby affecting the growth and development of rice and the number of tillers.

Indexed as

OryzaAmino AcidsGene EditingGene Expression ProfilingPlant DevelopmentAmino AcidsCOP9 signalosomeHeightOsCSN2RiceTiller number

Identifiers

PMID38381201
OpenAlexW4392003338

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.