Evidence map›Paper›PMID 30630423›Full record

ArticleBMC genomics2019

The genome-wide transcriptional consequences of the nullisomic-tetrasomic stocks for homoeologous group 7 in bread wheat.

Rongzhi Zhang, Shuaifeng Geng, Zhengrui Qin, Zongxiang Tang, Cheng Liu, Dongfeng Liu, Guoqi Song, Yulian Li, Shujuan Zhang, Wei Li and 3 more

Abstract read
In one paragraph

Article in BMC genomics, 2019. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Wheat-Frontiers in plant science · 2022
    Article
  3. 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

13 authors.

Rongzhi ZhangKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China. zhangrongzhi1981@126.com.
Shuaifeng GengInstitute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Zhengrui QinInstitute of Crop Science, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Zongxiang TangAgronomy College, Sichuan Agricultural University, Wenjiang, Chengdu, 610054, China.
Cheng LiuKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China.
Dongfeng LiuKey Laboratory of Plant Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Guoqi SongKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China.
Yulian LiKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China.
Shujuan ZhangKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China.
Wei LiKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China.
Jie GaoKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China.
Xiaodong HanKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China.
Genying LiKey Laboratory of Wheat Biology & Genetic Improvement on North Yellow & Huai River Valley, Ministry of Agriculture, National Engineering Laboratory for Wheat & Maize, Institute of Crop Science, Shandong Academy of Agricultural Sciences (SAAS), #202, Road of Gongyebei, Jinan, 250100, China. lgy111@126.com.

Funding

Key R&D Programme of Shandong Province 2017GNC10113Ministry of Agriculture of China 2018ZX08009-10Bthe Agricultural Science and Technology Innovation Project of Shandong Academy of Agricultural Sciences CXGC2016C09the Ministry of Science and Technology of China 2016YFD0100500The National Natural Science Foundation of China 31501312The National Natural Science Foundation of China 31601301The National Natural Science Foundation of China 31701428the Natural Science Foundation of Shandong Province ZR2014CM006the Youth Foundation of Shandong Academy of Agricultural Sciences 2016YQN01
6 · The paper itself

Abstract

backgroundHexaploid bread wheat (Triticum aestivum L) arose by two polyploidisation events from three diploid species with homoeologous genomes. Nullisomic-tetrasomic (nulli-tetra or NT) lines are aneuploid wheat plants lacking two and adding two of six homoeologous chromosomes. These plants can grow normally, but with significantly morphological variations because the adding two chromosomes or the remaining four chromosomes compensate for those absent. Despite these interesting phenomena, detailed molecular mechanisms underlying dosage deletion and compensation in these useful genetic materials have not been determined.

resultsBy sequencing the transcriptomes of leaves in two-week-old seedlings, we showed that the profiles of differentially expressed genes between NT stocks for homoeologous group 7 and the parent hexaploid Chinese Spring (CS) occurred throughout the whole genome with a subgenome and chromosome preference. The deletion effect of nulli-chromosomes was compensated partly by the tetra-chromosomes via the dose level of expressed genes, according to the types of homoeologous genes. The functions of differentially regulated genes primarily focused on carbon metabolic process, photosynthesis process, hormone metabolism, and responding to stimulus, and etc., which might be related to the defective phenotypes that included reductions in plant height, flag leaf length, spikelet number, and kernels per spike.

conclusionsThe perturbation of the expression levels of transcriptional genes among the NT stocks for homoeologous group 7 demonstrated the gene dosage effect of the subgenome at the genome-wide level. The gene dosage deletion and compensation can be used as a model to elucidate the functions of the subgenomes in modern polyploid plants.

Indexed as

BreadGene DosageGene ExpressionPolyploidyTranscriptomeAneuploidyChromosome MappingChromosomes, PlantGenes, PlantSeedlingsTriticumDosage compensationDosage deletionGene expressionNullisomic-tetrasomic stocksTriticum aestivum L

Identifiers

PMID30630423
PMCPMC6327598

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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 OpenQuestion graph.