Evidence map›Paper›PMID 32297039›Full record

ArticleRice (New York, N.Y.)2020

OsSLC1 Encodes a Pentatricopeptide Repeat Protein Essential for Early Chloroplast Development and Seedling Survival.

Jun Lv, Lianguang Shang, Yun Chen, Yao Han, Xiaoyan Yang, Shuzhang Xie, Wenqin Bai, Mingyu Hu, Hong Wu, Kairong Lei and 6 more

Open access · goldAbstract read
In one paragraph

Article in Rice (New York, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 40 citations in OpenAlex.

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  16. Frontiers in plant science · 2021
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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

16 authors at 6 institutions in 1 country.

Jun LvCollege of Agronomy and Biotechnology, Southwest University, Chongqing, 400715, China.
Lianguang ShangShenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518124, China.
Yun ChenState Key Laboratory for Conservation and Utilization of Bio-resources in Yunnan, Research Center for Perennial Rice Engineering and Technology in Yunnan, School of Agriculture, Yunnan University, Kunming, 650500, China.
Yao HanChongqing Key Laboratory of Adversity Agriculture Research, Biotechnology Research Center, Chongqing Academy of Agricultural Sciences, Chongqing, 401329, China.
Xiaoyan YangChongqing Key Laboratory of Adversity Agriculture Research, Biotechnology Research Center, Chongqing Academy of Agricultural Sciences, Chongqing, 401329, China.
Shuzhang XieChongqing Key Laboratory of Adversity Agriculture Research, Biotechnology Research Center, Chongqing Academy of Agricultural Sciences, Chongqing, 401329, China.
Wenqin BaiChongqing Key Laboratory of Adversity Agriculture Research, Biotechnology Research Center, Chongqing Academy of Agricultural Sciences, Chongqing, 401329, China.
Mingyu HuChongqing Key Laboratory of Adversity Agriculture Research, Biotechnology Research Center, Chongqing Academy of Agricultural Sciences, Chongqing, 401329, China.
Hong WuChongqing Key Laboratory of Adversity Agriculture Research, Biotechnology Research Center, Chongqing Academy of Agricultural Sciences, Chongqing, 401329, China.
Kairong LeiChongqing Key Laboratory of Adversity Agriculture Research, Biotechnology Research Center, Chongqing Academy of Agricultural Sciences, Chongqing, 401329, China.
Ya'nan YangShenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture, Genome Analysis Laboratory of the Ministry of Agriculture, Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, 518124, China.
Shengzhen GeCollege of Agronomy and Biotechnology, Southwest University, Chongqing, 400715, China.
Hai Phuong TrinhCollege of Agronomy and Biotechnology, Southwest University, Chongqing, 400715, China.
Yi ZhangState Key Laboratory for Conservation and Utilization of Bio-resources in Yunnan, Research Center for Perennial Rice Engineering and Technology in Yunnan, School of Agriculture, Yunnan University, Kunming, 650500, China.
Longbiao GuoState Key Laboratory of Rice Biology, China National Rice Research Institute, Zhejiang, 310006, China.
Zhongwei WangChongqing Key Laboratory of Adversity Agriculture Research, Biotechnology Research Center, Chongqing Academy of Agricultural Sciences, Chongqing, 401329, China. shengran4@126.com.
Chongqing Academy of Agricultural Sciences · CNSouthwest University · CNChina National Rice Research Institute · CNYunnan University · CNAgricultural Genomics Institute at Shenzhen · CNChinese Academy of Agricultural Sciences · CN

Funding

the Agricultural Science and Technology Innovation Program, Shenzhen Science and Technology Program No.2017050414212249the Foundation of Discovery and Utilization of Green, High-quality and High-efficiency Rice Germplasm Resources NKY-2018QC03the Fundamental Research Funds of Chongqing 2016cstc-jbky-00524the National Natural Science Foundation of China 31370349the National Natural Science Foundation of China 31701390the Project on Basic Research and Frontier Exploration of Chongqing cstc2018jcyjAX0234the Special Project on Performance Incentive Guidance of Chongqing Scientific Research Institution cstc2018jxjl80021
6 · The paper itself

Abstract

backgroundThe large family of pentatricopeptide repeat (PPR) proteins is widely distributed among land plants. Such proteins play vital roles in intron splicing, RNA editing, RNA processing, RNA stability and RNA translation. However, only a small number of PPR genes have been identified in rice.

resultsIn this study, we raised a mutant from tissue-culture-derived plants of Oryza sativa subsp. japonica 'Zhonghua 11', which exhibited a lethal chlorosis phenotype from germination to the third-leaf stage. The mutant was designated seedling-lethal chlorosis 1 (slc1). The slc1 mutant leaves showed extremely low contents of photosynthetic pigments and abnormal chloroplast development, and were severely defective in photosynthesis. Map-based cloning of OsSLC1 revealed that a single base (G) deletion was detected in the first exon of Os06g0710800 in the slc1 mutant, which caused a premature stop codon. Knockout and complementation experiments further confirmed that OsSLC1 is responsible for the seedling-lethal chlorosis phenotype in the slc1 mutant. OsSLC1 was preferentially expressed in green leaves, and encoded a chloroplast-localized PPR protein harboring 12 PPR motifs. Loss-of-function of OsSLC1 affected the intron splicing of multiple group II introns, and especially precluded the intron splicing of rps16, and resulted in significant increase in the transcript levels of 3 chloroplast ribosomal RNAs and 16 chloroplast development-related and photosynthesis-related genes, and in significant reduction in the transcript levels of 1 chloroplast ribosomal RNAs and 2 chloroplast development-related and photosynthesis-related genes.

conclusionWe characterized a novel chloroplast-localized PPR protein, OsSLC1, which plays a vital role in the intron splicing of multiple group II introns, especially the rps16 intron, and is essential for early chloroplast development and seedling survival in rice.

Indexed as

Chloroplast developmentChlorosis phenotypeIntron splicingOryza sativaPPR protein

Identifiers

PMID32297039
PMCPMC7160225
OpenAlexW3016751290

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.