Comparative Transcriptome Analysis of Gene Expression Patterns in Tomato Under Dynamic Light Conditions.

Abstract:

:Plants grown under highly variable natural light regimes differ strongly from plants grown under constant light (CL) regimes. Plant phenotype and adaptation responses are important for plant biomass and fitness. However, the underlying regulatory mechanisms are still poorly understood, particularly from a transcriptional perspective. To investigate the influence of different light regimes on tomato plants, three dynamic light (DL) regimes were designed, using a CL regime as control. Morphological, photosynthetic, and transcriptional differences after five weeks of treatment were compared. Leaf area, plant height, shoot /root weight, total chlorophyll content, photosynthetic rate, and stomatal conductance all significantly decreased in response to DL regimes. The biggest expression difference was found between the treatment with the highest light intensity at the middle of the day with a total of 1080 significantly up-/down-regulated genes. A total of 177 common differentially expressed genes were identified between DL and CL conditions. Finally, significant differences were observed in the levels of gene expression between DL and CL treatments in multiple pathways, predominantly of plant-pathogen interactions, plant hormone signal transductions, metabolites, and photosynthesis. These results expand the understanding of plant development and photosynthetic regulations under DL conditions by multiple pathways.

journal_name

Genes (Basel)

journal_title

Genes

authors

Ding J,Zhao J,Pan T,Xi L,Zhang J,Zou Z

doi

10.3390/genes10090662

subject

Has Abstract

pub_date

2019-08-29 00:00:00

issue

9

issn

2073-4425

pii

genes10090662

journal_volume

10

pub_type

杂志文章

相关文献

Genes文献大全
  • High-Throughput Genetic Testing in ALS: The Challenging Path of Variant Classification Considering the ACMG Guidelines.

    abstract::The development of high-throughput sequencing technologies and screening of big patient cohorts with familial and sporadic amyotrophic lateral sclerosis (ALS) led to the identification of a significant number of genetic variants, which are sometimes difficult to interpret. The American College of Medical Genetics and ...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11101123

    authors: Lattante S,Marangi G,Doronzio PN,Conte A,Bisogni G,Zollino M,Sabatelli M

    更新日期:2020-09-24 00:00:00

  • Molecular Processes Connecting DNA Methylation Patterns with DNA Methyltransferases and Histone Modifications in Mammalian Genomes.

    abstract::DNA methylation is an essential part of the epigenome chromatin modification network, which also comprises several covalent histone protein post-translational modifications. All these modifications are highly interconnected, because the writers and erasers of one mark, DNA methyltransferases (DNMTs) and ten eleven tra...

    journal_title:Genes

    pub_type: 杂志文章,评审

    doi:10.3390/genes9110566

    authors: Jeltsch A,Broche J,Bashtrykov P

    更新日期:2018-11-21 00:00:00

  • Genome Sequencing and Assembly by Long Reads in Plants.

    abstract::Plant genomes generated by Sanger and Next Generation Sequencing (NGS) have provided insight into species diversity and evolution. However, Sanger sequencing is limited in its applications due to high cost, labor intensity, and low throughput, while NGS reads are too short to resolve abundant repeats and polyploidy, l...

    journal_title:Genes

    pub_type: 杂志文章,评审

    doi:10.3390/genes9010006

    authors: Li C,Lin F,An D,Wang W,Huang R

    更新日期:2017-12-28 00:00:00

  • Epitranscriptomic Signatures in lncRNAs and Their Possible Roles in Cancer.

    abstract::In contrast to the amazing exponential growth in knowledge related to long non-coding RNAs (lncRNAs) involved in cell homeostasis or dysregulated pathological states, little is known so far about the links between the chemical modifications occurring in lncRNAs and their function. Generally, ncRNAs are post-transcript...

    journal_title:Genes

    pub_type: 杂志文章,评审

    doi:10.3390/genes10010052

    authors: Dinescu S,Ignat S,Lazar AD,Constantin C,Neagu M,Costache M

    更新日期:2019-01-16 00:00:00

  • From Structural Variation of Gene Molecules to Chromatin Dynamics and Transcriptional Bursting.

    abstract::Transcriptional activation of eukaryotic genes is accompanied, in general, by a change in the sensitivity of promoter chromatin to endonucleases. The structural basis of this alteration has remained elusive for decades; but the change has been viewed as a transformation of one structure into another, from "closed" to ...

    journal_title:Genes

    pub_type: 杂志文章,评审

    doi:10.3390/genes6030469

    authors: Boeger H,Shelansky R,Patel H,Brown CR

    更新日期:2015-06-30 00:00:00

  • Genome-Wide Profiling of Enterotoxigenic Staphylococcus aureus Strains Used for the Production of Naturally Contaminated Cheeses.

    abstract::Staphylococcus aureus is a major human pathogen and an important cause of livestock infections. More than 20 staphylococcal enterotoxins with emetic activity can be produced by specific strains responsible for staphylococcal food poisoning, one of the most common food-borne diseases. Whole genome sequencing provides a...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11010033

    authors: Macori G,Bellio A,Bianchi DM,Chiesa F,Gallina S,Romano A,Zuccon F,Cabrera-Rubio R,Cauquil A,Merda D,Auvray F,Decastelli L

    更新日期:2019-12-27 00:00:00

  • Cord Blood DNA Methylation Biomarkers for Predicting Neurodevelopmental Outcomes.

    abstract::Adverse environmental exposures in pregnancy can significantly alter the development of the fetus resulting in impaired child neurodevelopment. Such exposures can lead to epigenetic alterations like DNA methylation, which may be a marker of poor cognitive, motor and behavioral outcomes in the infant. Here we review st...

    journal_title:Genes

    pub_type: 杂志文章,评审

    doi:10.3390/genes7120117

    authors: Hodyl NA,Roberts CT,Bianco-Miotto T

    更新日期:2016-12-03 00:00:00

  • RNA-Seq Analyses Identify Additivity as the Predominant Gene Expression Pattern in F1 Chicken Embryonic Brain and Liver.

    abstract::The superior performance of hybrids to parents, termed heterosis, has been widely utilized in animal and plant breeding programs, but the molecular mechanism underlying heterosis remains an enigma. RNA-Seq provides a novel way to investigate heterosis at the transcriptome-wide level, because gene expression functions ...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes10010027

    authors: Zhuo Z,Lamont SJ,Abasht B

    更新日期:2019-01-07 00:00:00

  • Exposure to Formaldehyde Perturbs the Mouse Gut Microbiome.

    abstract::Exposure to Formaldehyde (FA) results in many pathophysiological symptoms, however the underlying mechanisms are not well understood. Given the complicated modulatory role of intestinal microbiota on human health, we hypothesized that interactions between FA and the gut microbiome may account for FA's toxicity. Balb/c...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes9040192

    authors: Guo J,Zhao Y,Jiang X,Li R,Xie H,Ge L,Xie B,Yang X,Zhang L

    更新日期:2018-04-03 00:00:00

  • Germination-Arrest Bacillus subtilis Spores as An Oral Delivery Vehicle of Grass Carp Reovirus (GCRV) Vp7 Antigen Augment Protective Immunity in Grass Carp (Ctenopharyngodon idella).

    abstract::Oral vaccination is a practical method for the active immunization of farmed fish in the matter of animal welfare and handling costs. However, it always shows insufficient protective immunity, mainly due to antigen degradation in the gastrointestinal tract (GIT). Bacillus subtilis spores have been shown to be able to ...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11111351

    authors: Sun R,Zhang M,Chen H,Wei Y,Ning D

    更新日期:2020-11-14 00:00:00

  • Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-Onset Progressive Hearing Loss.

    abstract::MYO6 is known as a genetic cause of autosomal dominant and autosomal recessive inherited hearing loss. In this study, to clarify the frequency and clinical characteristics of hearing loss caused by MYO6 gene mutations, a large-scale genetic analysis of Japanese patients with hearing loss was performed. By means of mas...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11030273

    authors: Oka SI,Day TF,Nishio SY,Moteki H,Miyagawa M,Morita S,Izumi S,Ikezono T,Abe S,Nakayama J,Hyogo M,Okamoto N,Uehara N,Oshikawa C,Kitajiri SI,Usami SI

    更新日期:2020-03-04 00:00:00

  • Genome-Wide Identification and Characterization of Xyloglucan Endotransglycosylase/Hydrolase in Ananas comosus during Development.

    abstract::Xyloglucan endotransglycosylase/hydrolase (XTH) is a cell-wall-modifying enzyme participating in diverse cell morphogenetic processes and adaptation to stress. In this study, 48 XTH genes were identified from two pineapple (Ananas comosus) cultivars ('F153' and 'MD2') and designated Ac(F153)XTH1 to -24 and Ac(MD2)XTH1...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes10070537

    authors: Li Q,Li H,Yin C,Wang X,Jiang Q,Zhang R,Ge F,Chen Y,Yang L

    更新日期:2019-07-16 00:00:00

  • Unmasking Intra-tumoral Heterogeneity and Clonal Evolution in NF1-MPNST.

    abstract::Sarcomas are highly aggressive cancers that have a high propensity for metastasis, fail to respond to conventional therapies, and carry a poor 5-year survival rate. This is particularly true for patients with neurofibromatosis type 1 (NF1), in which 8%-13% of affected individuals will develop a malignant peripheral ne...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11050499

    authors: Moon CI,Tompkins W,Wang Y,Godec A,Zhang X,Pipkorn P,Miller CA,Dehner C,Dahiya S,Hirbe AC

    更新日期:2020-05-01 00:00:00

  • Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome.

    abstract::Epigenetic alterations at imprinted genes on different chromosomes have been linked to several imprinting disorders (IDs) such as Beckwith-Wiedemann syndrome (BWS) and pseudohypoparathyroidism type 1b (PHP1b). Here, we present a male patient with these two distinct IDs caused by two independent mechanisms-loss of meth...

    journal_title:Genes

    pub_type:

    doi:10.3390/genes12020172

    authors: Choufani S,Ko JM,Lou Y,Shuman C,Fishman L,Weksberg R

    更新日期:2021-01-27 00:00:00

  • A Semi-Supervised Learning Algorithm for Predicting Four Types MiRNA-Disease Associations by Mutual Information in a Heterogeneous Network.

    abstract::Increasing evidence suggests that dysregulation of microRNAs (miRNAs) may lead to a variety of diseases. Therefore, identifying disease-related miRNAs is a crucial problem. Currently, many computational approaches have been proposed to predict binary miRNA-disease associations. In this study, in order to predict under...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes9030139

    authors: Zhang X,Yin J,Zhang X

    更新日期:2018-03-02 00:00:00

  • Dysregulated MicroRNA Expression Profiles and Potential Cellular, Circulating and Polymorphic Biomarkers in Non-Hodgkin Lymphoma.

    abstract::A large number of studies have focused on identifying molecular biomarkers, including microRNAs (miRNAs) to aid in the diagnosis and prognosis of the most common subtypes of non-Hodgkin lymphoma (NHL), Diffuse Large B-cell Lymphoma and Follicular Lymphoma. NHL is difficult to diagnose and treat with many cases becomin...

    journal_title:Genes

    pub_type: 杂志文章,评审

    doi:10.3390/genes7120130

    authors: Bradshaw G,Sutherland HG,Haupt LM,Griffiths LR

    更新日期:2016-12-17 00:00:00

  • Differential DNA Methylation Landscape in Skin Fibroblasts from African Americans with Systemic Sclerosis.

    abstract::The etiology and reasons underlying the ethnic disparities in systemic sclerosis (SSc) remain unknown. African Americans are disproportionally affected by SSc and yet are underrepresented in research. The aim of this study was to comprehensively investigate the association of DNA methylation levels with SSc in dermal ...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes12020129

    authors: Baker Frost D,da Silveira W,Hazard ES,Atanelishvili I,Wilson RC,Flume J,Day KL,Oates JC,Bogatkevich GS,Feghali-Bostwick C,Hardiman G,Ramos PS

    更新日期:2021-01-20 00:00:00

  • The Genome of the Northern Sea Otter (Enhydra lutris kenyoni).

    abstract::The northern sea otter inhabits coastal waters of the northern Pacific Ocean and is the largest member of the Mustelidae family. DNA sequencing methods that utilize microfluidic partitioned and non-partitioned library construction were used to establish the sea otter genome. The final assembly provided 2.426 Gbp of hi...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes8120379

    authors: Jones SJ,Haulena M,Taylor GA,Chan S,Bilobram S,Warren RL,Hammond SA,Mungall KL,Choo C,Kirk H,Pandoh P,Ally A,Dhalla N,Tam AKY,Troussard A,Paulino D,Coope RJN,Mungall AJ,Moore R,Zhao Y,Birol I,Ma Y,Marra M,Jo

    更新日期:2017-12-11 00:00:00

  • Genome-Wide Identification of Na+/H+ Antiporter (NHX) Genes in Sugar Beet (Beta vulgaris L.) and Their Regulated Expression under Salt Stress.

    abstract::Salinity is one of the major environment factors that limits the growth of plants and the productivity of crops worldwide. It has been shown that Na+ transporters play a central role in salt tolerance and development of plants. The objective of this study was to identify Na+/H+ antiporter (NHX) genes and investigate t...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes10050401

    authors: Wu GQ,Wang JL,Li SJ

    更新日期:2019-05-27 00:00:00

  • Abnormal base excision repair at trinucleotide repeats associated with diseases: a tissue-selective mechanism.

    abstract::More than fifteen genetic diseases, including Huntington's disease, myotonic dystrophy 1, fragile X syndrome and Friedreich ataxia, are caused by the aberrant expansion of a trinucleotide repeat. The mutation is unstable and further expands in specific cells or tissues with time, which can accelerate disease progressi...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes4030375

    authors: Goula AV,Merienne K

    更新日期:2013-07-25 00:00:00

  • Evolutionary Insights of the ZW Sex Chromosomesin Snakes: A New Chapter Added by the AmazonianPuffing Snakes of the Genus Spilotes.

    abstract::Amazonian puffing snakes (Spilotes; Colubridae) are snakes widely distributed in the Neotropical region. However, chromosomal data are scarce in this group and, when available, are only limited to karyotype description using conventional staining. In this paper, we focused on the process of karyotype evolution and tre...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes10040288

    authors: Viana PF,Ezaz T,de Bello Cioffi M,Jackson Almeida B,Feldberg E

    更新日期:2019-04-09 00:00:00

  • Genome-Wide Identification of lncRNAs During Rice Seed Development.

    abstract::Rice seed is a pivotal reproductive organ that directly determines yield and quality. Long non-coding RNAs (lncRNAs) have been recognized as key regulators in plant development, but the roles of lncRNAs in rice seed development remain unclear. In this study, we performed a paired-end RNA sequencing in samples of rice ...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11030243

    authors: Zhao J,Ajadi AA,Wang Y,Tong X,Wang H,Tang L,Li Z,Shu Y,Liu X,Li S,Wang S,Liu W,Zhang J

    更新日期:2020-02-26 00:00:00

  • Effects of 5'-3' Exonuclease Xrn1 on Cell Size, Proliferation and Division, and mRNA Levels of Periodic Genes in Cryptococcus neoformans.

    abstract::Cell size affects almost all biosynthetic processes by controlling the size of organelles and disrupting the nutrient uptake process. Yeast cells must reach a critical size to be able to enter a new cell cycle stage. Abnormal changes in cell size are often observed under pathological conditions such as cancer disease....

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11040430

    authors: Zhao X,Li X,Zhang P,Li C,Feng W,Zhu X,Wei D

    更新日期:2020-04-16 00:00:00

  • NetR and AttR, Two New Bioinformatic Tools to Integrate Diverse Datasets into Cytoscape Network and Attribute Files.

    abstract::High-throughput technologies have allowed researchers to obtain genome-wide data from a wide array of experimental model systems. Unfortunately, however, new data generation tends to significantly outpace data re-utilization, and most high throughput datasets are only rarely used in subsequent studies or to generate n...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes10060423

    authors: Halajyan A,Weingart N,Yeahia M,Loza-Coll M

    更新日期:2019-06-01 00:00:00

  • Transcriptome Analysis Reveals Inhibitory Effects of Lentogenic Newcastle Disease Virus on Cell Survival and Immune Function in Spleen of Commercial Layer Chicks.

    abstract::As a major infectious disease in chickens, Newcastle disease virus (NDV) causes considerable economic losses in the poultry industry, especially in developing countries where there is limited access to effective vaccination. Therefore, enhancing resistance to the virus in commercial chickens through breeding is a prom...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11091003

    authors: Zhang J,Kaiser MG,Gallardo RA,Kelly TR,Dekkers JCM,Zhou H,Lamont SJ

    更新日期:2020-08-26 00:00:00

  • A Magnesium Transport Protein Related to Mammalian SLC41 and Bacterial MgtE Contributes to Circadian Timekeeping in a Unicellular Green Alga.

    abstract::Circadian clocks in eukaryotes involve both transcriptional-translational feedback loops, post-translational regulation, and metabolic, non-transcriptional oscillations. We recently identified the involvement of circadian oscillations in the intracellular concentrations of magnesium ions (Mg2+i) that were conserved in...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes10020158

    authors: Feord HK,Dear FEG,Obbard DJ,van Ooijen G

    更新日期:2019-02-19 00:00:00

  • Testosterone Degradative Pathway of Novosphingobium tardaugens.

    abstract::In this work, we have shown that Novosphingobium tardaugens NBRC 16725 (strain ARI-1), a bacterial strain that was isolated due to its capacity to mineralize the estrogenic endocrine compound 17β-estradiol, is also able to mineralize testosterone, the androgenic endocrine compound. Using in silico analysis, we predict...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes10110871

    authors: Ibero J,Galán B,Díaz E,García JL

    更新日期:2019-10-31 00:00:00

  • Rapid Direct Nucleic Acid Amplification Test without RNA Extraction for SARS-CoV-2 Using a Portable PCR Thermocycler.

    abstract::There is an ongoing worldwide coronavirus disease 2019 (Covid-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). At present, confirmatory diagnosis is by reverse transcription polymerase chain reaction (RT-PCR), typically taking several hours and requiring a molecular laboratory to pe...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11060664

    authors: Wee SK,Sivalingam SP,Yap EPH

    更新日期:2020-06-18 00:00:00

  • Regulation of the X Chromosome in the Germline and Soma of Drosophila melanogaster Males.

    abstract::During the evolution of heteromorphic sex chromosomes, the sex-specific Y chromosome degenerates, while the X chromosome evolves new mechanisms of regulation. Using bioinformatic and experimental approaches, we investigate the expression of the X chromosome in Drosophila melanogaster. We observe nearly complete X chro...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes9050242

    authors: Argyridou E,Parsch J

    更新日期:2018-05-04 00:00:00

  • Phylogenetic Analysis and Karyotype Evolution in Two Species of Core Gruiformes: Aramides cajaneus and Psophia viridis.

    abstract::Gruiformes is a group with phylogenetic issues. Recent studies based on mitochondrial and genomic DNA have proposed the existence of a core Gruiformes, consisting of five families: Heliornithidae, Aramidae, Gruidae, Psophiidae and Rallidae. Karyotype studies on these species are still scarce, either by conventional st...

    journal_title:Genes

    pub_type: 杂志文章

    doi:10.3390/genes11030307

    authors: Furo IO,Kretschmer R,O'Brien PCM,Pereira JC,Ferguson-Smith MA,de Oliveira EHC

    更新日期:2020-03-13 00:00:00