scholarly journals Evolutionary Analysis of the YABBY Gene Family in Brassicaceae

Plants ◽  
2021 ◽  
Vol 10 (12) ◽  
pp. 2700
Author(s):  
Yun-Hai Lu ◽  
Intikhab Alam ◽  
Yan-Qing Yang ◽  
Ya-Cen Yu ◽  
Wen-Chao Chi ◽  
...  
Keyword(s):  
Gene Family ◽  
Phylogenetic Analyses ◽  
Functional Characterization ◽  
Brassica Species ◽  
Variable Number ◽  
Evolutionary Analysis ◽  
Brassicaceae Species ◽  
Yabby Gene ◽  
Stress Signals ◽  
Evolutionary Story

The YABBY gene family is one of the plant transcription factors present in all seed plants. The family members were extensively studied in various plants and shown to play important roles in plant growth and development, such as the polarity establishment in lateral organs, the formation and development of leaves and flowers, and the response to internal plant hormone and external environmental stress signals. In this study, a total of 364 YABBY genes were identified from 37 Brassicaceae genomes, of which 15 were incomplete due to sequence gaps, and nine were imperfect (missing C2C2 zinc-finger or YABBY domain) due to sequence mutations. Phylogenetic analyses resolved these YABBY genes into six compact clades except for a YAB3-like gene identified in Aethionema arabicum. Seventeen Brassicaceae species each contained a complete set of six basic YABBY genes (i.e., 1 FIL, 1 YAB2, 1 YAB3, 1 YAB5, 1 INO and 1 CRC), while 20 others each contained a variable number of YABBY genes (5–25) caused mainly by whole-genome duplication/triplication followed by gene losses, and occasionally by tandem duplications. The fate of duplicate YABBY genes changed considerably according to plant species, as well as to YABBY gene type. These YABBY genes were shown to be syntenically conserved across most of the Brassicaceae species, but their functions might be considerably diverged between species, as well as between paralogous copies, as demonstrated by the promoter and expression analysis of YABBY genes in two Brassica species (B. rapa and B. oleracea). Our study provides valuable insights for understanding the evolutionary story of YABBY genes in Brassicaceae and for further functional characterization of each YABBY gene across the Brassicaceae species.

scholarly journals Carotenoid Cleavage Dioxygenases: Identification, Expression, and Evolutionary Analysis of This Gene Family in Tobacco

2019 ◽  
Vol 20 (22) ◽  
pp. 5796
Author(s):  
Qianqian Zhou ◽  
Qingchang Li ◽  
Peng Li ◽  
Songtao Zhang ◽  
Che Liu ◽  
...  
Keyword(s):  
Gene Family ◽  
Physiological Stress ◽  
Expression Patterns ◽  
Functional Characterization ◽  
Hormone Treatment ◽  
Nicotiana Sylvestris ◽  
Regulatory Elements ◽  
Evolutionary Analysis ◽  
Comprehensive Overview ◽  
Carotenoid Cleavage Dioxygenases

Carotenoid cleavage dioxygenases (CCDs) selectively catalyze carotenoids, forming smaller apocarotenoids that are essential for the synthesis of apocarotenoid flavor, aroma volatiles, and phytohormone ABA/SLs, as well as responses to abiotic stresses. Here, 19, 11, and 10 CCD genes were identified in Nicotiana tabacum, Nicotiana tomentosiformis, and Nicotiana sylvestris, respectively. For this family, we systematically analyzed phylogeny, gene structure, conserved motifs, gene duplications, cis-elements, subcellular and chromosomal localization, miRNA-target sites, expression patterns with different treatments, and molecular evolution. CCD genes were classified into two subfamilies and nine groups. Gene structures, motifs, and tertiary structures showed similarities within the same groups. Subcellular localization analysis predicted that CCD family genes are cytoplasmic and plastid-localized, which was confirmed experimentally. Evolutionary analysis showed that purifying selection dominated the evolution of these genes. Meanwhile, seven positive sites were identified on the ancestor branch of the tobacco CCD subfamily. Cis-regulatory elements of the CCD promoters were mainly involved in light-responsiveness, hormone treatment, and physiological stress. Different CCD family genes were predominantly expressed separately in roots, flowers, seeds, and leaves and exhibited divergent expression patterns with different hormones (ABA, MeJA, IAA, SA) and abiotic (drought, cold, heat) stresses. This study provides a comprehensive overview of the NtCCD gene family and a foundation for future functional characterization of individual genes.

scholarly journals Genome-Wide Identification and Expression Analysis of Sucrose Nonfermenting-1-Related Protein Kinase (SnRK) Genes in Triticum aestivum in Response to Abiotic Stress

2021 ◽  
Author(s):  
Shefali Mishra ◽  
Pradeep Sharma ◽  
Rajender Singh ◽  
ratan Tiwari ◽  
Gyanendra Pratap Singh
Keyword(s):  
Triticum Aestivum ◽  
Gene Family ◽  
Structural Characteristics ◽  
Phylogenetic Analyses ◽  
Expression Patterns ◽  
Functional Characterization ◽  
Plant Stress ◽  
Protein Motif ◽  
Genome Wide

The SnRK gene family is a key regulator playing an important role in plant stress response by phosphorylating the target protein to regulate the signalling pathways. The function of SnRK gene family has been reported in many species but is limited to Triticum asetivum. In this study, SnRK gene family in the wheat genome was identified and its structural characteristics were described. One hundred forty-seven SnRK genes distributed across 21 chromosomes were identified in the Triticum aestivum genome and categorised into three subgroups (SnRK1/2/3) based on phylogenetic analyses and domain types. The gene intron-exon structure and protein-motif composition of SnRKs were similar within each subgroup but different amongst the groups. Gene duplication between the wheat, Arabidopsis, rice and barley genomes was also investigated in order to get insight into the evolutionary aspects of the TaSnRK family genes. SnRK genes showed differential expression patterns in leaves, roots, spike, and grains. Redundant stress-related cis-elements were also found in the promoters of 129 SnRK genes and their expression levels varied widely following drought, ABA and light regulated elements. In particular, TaSnRK2.11 had higher and increased expression under the abiotic stresses and can be a candidate gene for the abiotc stress tolerance. The findings will aid in the functional characterization of TaSnRK genes for further research.

Nuclear Factor-Y (NF-Y), the Key Player in Plant Growth and Development: Prediction and Characterization in Vanilla planifolia

2020 ◽  
Vol 09 ◽  
Author(s):  
Saavi Arora ◽  
Devina Ghai ◽  
Jaspreet K Sembi
Keyword(s):  
Gene Family ◽  
Growth And Development ◽  
Functional Characterization ◽  
Evolutionary Relationship ◽  
Dimensional Structure ◽  
Evolutionary Analysis ◽  
Nuclear Factor ◽  
Vanilla Planifolia ◽  
Variable Expression ◽  
Nuclear Factor Y

Background: V. planifolia is of tremendous commercial importance as a source of an important flavor, vanilla, which is the backbone of the culinary and perfumery industry. Hence, efforts to ease cultivation and promote growth in this plant are need of the hour. Nuclear factor-Y (NF-Y) gene family, a class of vital transcription factors, plays a pivotal role in a large number of developmental processes. Objectives: The present study aims to identify and characterize NF-Y gene family in Vanilla planifolia which would bring insights to their role as key factors promoting growth and development in this orchid. Methods: Physico-chemical characterization, protein structure prediction and interaction, establishment of evolutionary relationship and expression profiling were attempted using various in silico tools. Results: Twenty five putative NF-Y members were identified in Vanilla planifolia, which were further classified into three sub-classes, NF-YA (13), NF-YB (7) and NF-YC (5), on the basis of specific domains and conserved regions. Prediction of three dimensional structure was done on the basis of structural similarity with NF-Y structure templates. Evolutionary analysis with the NF-Ys of Arabidopsis thaliana and Oryza sativa, classified these into three major clusters which indicated towards similarity of functions. Variable expression of VpNF-Y genes confirmed their role in diverse functions. VpNF-YA genes generally showed higher expression in vegetative tissues while a few VpNF-YBs showed seed specific expression. Protein-protein interaction indicated complex formation for optimum function. Conclusions: This work paves way for further functional characterization of NF-Y genes in Vanilla planfolia.

scholarly journals Genome-Wide Analysis of the YABBY Gene Family in Grapevine and Functional Characterization of VvYABBY4

2019 ◽  
Vol 10 ◽  
Author(s):  
Songlin Zhang ◽  
Li Wang ◽  
Xiaomeng Sun ◽  
Yunduan Li ◽  
Jin Yao ◽  
...  
Keyword(s):  
Gene Family ◽  
Functional Characterization ◽  
Genome Wide Analysis ◽  
Genome Wide ◽  
Yabby Gene

scholarly journals Characterization of the GRAS gene family reveals their contribution to the high adaptability of wheat

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e10811
Author(s):  
Yanfeng Liu ◽  
Wei Wang
Keyword(s):  
Gene Family ◽  
Stress Responses ◽  
Epigenetic Modification ◽  
Phylogenetic Analyses ◽  
Draft Genome ◽  
High Rate ◽  
Segmental Duplications ◽  
Evolutionary Analysis ◽  
And Function ◽  
Gras Gene

GRAS transcription factors play important roles in many processes of plant development as well as abiotic and biotic stress responses. However, little is known about this gene family in bread wheat (Triticum aestivum), one of the most important crops worldwide. The completion of a quality draft genome allows genome-wide detection and evolutionary analysis of the GRAS gene family in wheat. In this study, 188 TaGRAS genes were detected and divided into 12 subfamilies based on phylogenetic analyses: DELLA, DLT, HAM, LISCL, SCL3, SCL4/7, SCR, SHR, PAT1, Os19, Os4 and LAS. Tandem and segmental duplications are the main contributors to the expansion of TaGRAS, which may contribute to the adaptation of wheat to various environmental conditions. A high rate of homoeolog retention during hexaploidization was detected, suggesting the nonredundancy and biological importance of TaGRAS homoeologs. Systematic analyses of TaGRAS indicated the conserved expression pattern and function of the same subfamily during evolution. In addition, we detected five genes belonging to the LISCL subfamily induced by both biotic and abiotic stresses and they may be potential targets for further research through gene editing. Using degradome and ChIP-seq data, we identified the targets of miR171 and histone modifications and further analyzed the contribution of epigenetic modification to the subfunctionalization of TaGRAS. This study laid a foundation for further functional elucidation of TaGRAS genes.

scholarly journals Evolutionary analysis of LP3 gene family in conifers: an ASR homolog

2020 ◽  
Author(s):  
Jonathan Lecoy ◽  
MR García-Gil
Keyword(s):  
Codon Usage ◽  
Gene Family ◽  
Loblolly Pine ◽  
Molecular Mechanisms ◽  
Selective Pressure ◽  
Phylogenetic Analyses ◽  
Acid Stress ◽  
Water Deficit Stress ◽  
Evolutionary Analysis ◽  
Translation Efficiency

AbstractDrought has long been established as a major environmental stress for plants which have in turn developed several coping strategies, ranging from physiological to molecular mechanisms. LP3; a homolog of the Abscisic Acid, Stress and Ripening (ASR) gene was first detected in tomato; and has been shown to be present in four different isoforms in loblolly pine called LP3-0, LP3-1, LP3-2 and LP3-3. While ASR has already been extensively studied notably in tomato, the same cannot be said of LP3. Like ASR, the different LP3 isoforms have been shown to be upregulated in response to water deficit stress and to also act as transcription factors for genes likely involved in hexose transport. In this study we have investigated the evolutionary history of LP3 gene family, with the aim of relating it to that of ASR from a phylogenetic perspective and comparing the differences in selective pressure and codon usage. Phylogenetic analyses of different LP3 homologs compared to ASR show that LP3 is less divergent across species than ASR and that even when comparing the different sub-sections of the gene the divergence rate of LP3 is lower than that of ASR. Analysis of different gene parameters showed that there were differences in GC1% and GC2% but not in total or GC3% content. All genes had a relatively high CAI value associated with a low to moderate ENC value, which is indicative of high translation efficiency found in highly expressed genes. Analysis of codon usage also showed that LP3 preferentially uses different codons than ASR. Selective pressure analysis across most of the LP3 and ASR genes used in this study showed that these genes were principally undergoing purifying selection, with the exception of LP3-3 which seems to be undergoing diversifying selection most probably due to the fact that it likely recently diverged from LP3-0. This study thus provides insight in how ASR and LP3 have diverged from each other while remaining homologous.

scholarly journals Comprehensive Genomic Analysis and Expression Profiling of Diacylglycerol Kinase (DGK) Gene Family in Soybean (Glycine max) under Abiotic Stresses

2019 ◽  
Vol 20 (6) ◽  
pp. 1361 ◽  
Author(s):  
Kue Carther ◽  
Toi Ketehouli ◽  
Nan Ye ◽  
Yan-Hai Yang ◽  
Nan Wang ◽  
...  
Keyword(s):  
Gene Family ◽  
Stress Responses ◽  
Expression Profiling ◽  
Phylogenetic Analyses ◽  
Functional Characterization ◽  
Genomic Analysis ◽  
Diacylglycerol Kinase ◽  
Soybean Genome ◽  
Pcr Analysis

Diacylglycerol kinase (DGK) is an enzyme that plays a pivotal role in abiotic and biotic stress responses in plants by transforming the diacylglycerol into phosphatidic acid. However, there is no report on the characterization of soybean DGK genes in spite of the availability of the soybean genome sequence. In this study, we performed genome-wide analysis and expression profiling of the DGK gene family in the soybean genome. We identified 12 DGK genes (namely GmDGK1-12) which all contained conserved catalytic domains with protein lengths and molecular weights ranging from 436 to 727 amino acids (aa) and 48.62 to 80.93 kDa, respectively. Phylogenetic analyses grouped GmDGK genes into three clusters—cluster I, cluster II, and cluster III—which had three, four, and five genes, respectively. The qRT-PCR analysis revealed significant GmDGK gene expression levels in both leaves and roots coping with polyethylene glycol (PEG), salt, alkali, and salt/alkali treatments. This work provides the first characterization of the DGK gene family in soybean and suggests their importance in soybean response to abiotic stress. These results can serve as a guide for future studies on the understanding and functional characterization of this gene family.

scholarly journals Genome-wide identification and expression analysis of sucrose nonfermenting-1-related protein kinase (SnRK) genes in Triticum aestivum in response to abiotic stress

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Shefali Mishra ◽  
Pradeep Sharma ◽  
Rajender Singh ◽  
Ratan Tiwari ◽  
Gyanendra Pratap Singh
Keyword(s):  
Abiotic Stress ◽  
Gene Family ◽  
Abiotic Stresses ◽  
Phylogenetic Analyses ◽  
Abiotic Stress Tolerance ◽  
Functional Characterization ◽  
Protein Motif ◽  
Element Analysis ◽  
Genome Wide ◽  
A Genome

AbstractThe SnRK gene family is a key regulator that plays an important role in plant stress response by phosphorylating the target protein to regulate subsequent signaling pathways. This study was aimed to perform a genome-wide analysis of the SnRK gene family in wheat and the expression profiling of SnRKs in response to abiotic stresses. An in silico analysis identified 174 SnRK genes, which were then categorized into three subgroups (SnRK1/2/3) on the basis of phylogenetic analyses and domain types. The gene intron–exon structure and protein-motif composition of SnRKs were similar within each subgroup but different amongst the groups. Gene duplication and synteny between the wheat and Arabidopsis genomes was also investigated in order to get insight into the evolutionary aspects of the TaSnRK family genes. The result of cis-acting element analysis showed that there were abundant stress- and hormone-related cis-elements in the promoter regions of 129 SnRK genes. Furthermore, quantitative real-time PCR data revealed that heat, salt and drought treatments enhanced TaSnRK2.11 expression, suggesting that it might be a candidate gene for abiotic stress tolerance. We also identified eight microRNAs targeting 16 TaSnRK genes which are playing important role across abiotic stresses and regulation in different pathways. These findings will aid in the functional characterization of TaSnRK genes for further research.

scholarly journals Molecular Phylogenetic Analysis of the AIG Family in Vertebrates

Genes ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 1190
Author(s):  
Yuqi Huang ◽  
Minghao Sun ◽  
Lenan Zhuang ◽  
Jin He
Keyword(s):  
Phylogenetic Analysis ◽  
Gene Family ◽  
Functional Characterization ◽  
Vertebrate Evolution ◽  
Molecular Phylogenetic Analysis ◽  
Whole Genome Duplications ◽  
Genome Duplications ◽  
Molecular Phylogenetic ◽  
Duplication Events ◽  
Inducible Genes

Androgen-inducible genes (AIGs), which can be regulated by androgen level, constitute a group of genes characterized by the presence of the AIG/FAR-17a domain in its protein sequence. Previous studies on AIGs demonstrated that one member of the gene family, AIG1, is involved in many biological processes in cancer cell lines and that ADTRP is associated with cardiovascular diseases. It has been shown that the numbers of AIG paralogs in humans, mice, and zebrafish are 2, 2, and 3, respectively, indicating possible gene duplication events during vertebrate evolution. Therefore, classifying subgroups of AIGs and identifying the homologs of each AIG member are important to characterize this novel gene family further. In this study, vertebrate AIGs were phylogenetically grouped into three major clades, ADTRP, AIG1, and AIG-L, with AIG-L also evident in an outgroup consisting of invertebrsate species. In this case, AIG-L, as the ancestral AIG, gave rise to ADTRP and AIG1 after two rounds of whole-genome duplications during vertebrate evolution. Then, the AIG family, which was exposed to purifying forces during evolution, lost or gained some of its members in some species. For example, in eutherians, Neognathae, and Percomorphaceae, AIG-L was lost; in contrast, Salmonidae and Cyprinidae acquired additional AIG copies. In conclusion, this study provides a comprehensive molecular phylogenetic analysis of vertebrate AIGs, which can be employed for future functional characterization of AIGs.

scholarly journals Genome-wide identification of sucrose nonfermenting-1-related protein kinase (SnRK) genes in barley and RNA-seq analyses of their expression in response to abscisic acid treatment

BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Zhiwei Chen ◽  
Longhua Zhou ◽  
Panpan Jiang ◽  
Ruiju Lu ◽  
Nigel G. Halford ◽  
...  
Keyword(s):  
Abscisic Acid ◽  
Gene Family ◽  
Stress Responses ◽  
Phylogenetic Analyses ◽  
Regulatory Elements ◽  
Gene Promoters ◽  
Related Protein ◽  
Rna Seq ◽  
Response Elements ◽  
Genome Data

Abstract Background Sucrose nonfermenting-1 (SNF1)-related protein kinases (SnRKs) play important roles in regulating metabolism and stress responses in plants, providing a conduit for crosstalk between metabolic and stress signalling, in some cases involving the stress hormone, abscisic acid (ABA). The burgeoning and divergence of the plant gene family has led to the evolution of three subfamilies, SnRK1, SnRK2 and SnRK3, of which SnRK2 and SnRK3 are unique to plants. Therefore, the study of SnRKs in crops may lead to the development of strategies for breeding crop varieties that are more resilient under stress conditions. In the present study, we describe the SnRK gene family of barley (Hordeum vulgare), the widespread cultivation of which can be attributed to its good adaptation to different environments. Results The barley HvSnRK gene family was elucidated in its entirety from publicly-available genome data and found to comprise 50 genes. Phylogenetic analyses assigned six of the genes to the HvSnRK1 subfamily, 10 to HvSnRK2 and 34 to HvSnRK3. The search was validated by applying it to Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa) genome data, identifying 50 SnRK genes in rice (four OsSnRK1, 11 OsSnRK2 and 35 OsSnRK3) and 39 in Arabidopsis (three AtSnRK1, 10 AtSnRK2 and 26 AtSnRK3). Specific motifs were identified in the encoded barley proteins, and multiple putative regulatory elements were found in the gene promoters, with light-regulated elements (LRE), ABA response elements (ABRE) and methyl jasmonate response elements (MeJa) the most common. RNA-seq analysis showed that many of the HvSnRK genes responded to ABA, some positively, some negatively and some with complex time-dependent responses. Conclusions The barley HvSnRK gene family is large, comprising 50 members, subdivided into HvSnRK1 (6 members), HvSnRK2 (10 members) and HvSnRK3 (34 members), showing differential positive and negative responses to ABA.

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