Identification of quantitative trait loci for ABA responsiveness at the seedling stage associated with ABA-regulated gene expression in common wheat

2010 ◽  
Vol 121 (4) ◽  
pp. 629-641 ◽  
Author(s):  
Fuminori Kobayashi ◽  
Shigeo Takumi ◽  
Hirokazu Handa
Plant Science ◽  
2006 ◽  
Vol 170 (1) ◽  
pp. 12-17 ◽  
Author(s):  
Yanjun Dong ◽  
H. Kamiuten ◽  
Zhongnan Yang ◽  
Dongzhi Lin ◽  
T. Ogawa ◽  
...  

Euphytica ◽  
2017 ◽  
Vol 213 (6) ◽  
Author(s):  
Jingyi Guo ◽  
Guangdeng Chen ◽  
Xizhou Zhang ◽  
Tingxuan Li ◽  
Haiying Yu ◽  
...  

Plants ◽  
2019 ◽  
Vol 8 (2) ◽  
pp. 33 ◽  
Author(s):  
Md. Islam ◽  
John Ontoy ◽  
Prasanta Subudhi

Soil and water salinity is one of the major abiotic stresses that reduce growth and productivity in major food crops including rice. The lack of congruence of salt tolerance quantitative trait loci (QTLs) in multiple genetic backgrounds and multiple environments is a major hindrance for undertaking marker-assisted selection (MAS). A genome-wide meta-analysis of QTLs controlling seedling-stage salt tolerance was conducted in rice using QTL information from 12 studies. Using a consensus map, 11 meta-QTLs for three traits with smaller confidence intervals were localized on chromosomes 1 and 2. The phenotypic variance of 3 meta-QTLs was ≥20%. Based on phenotyping of 56 diverse genotypes and breeding lines, six salt-tolerant genotypes (Bharathy, I Kung Ban 4-2 Mutant, Langmanbi, Fatehpur 3, CT-329, and IARI 5823) were identified. The perusal of the meta-QTL regions revealed several candidate genes associated with salt-tolerance attributes. The lack of association between meta-QTL linked markers and the level of salt tolerance could be due to the low resolution of meta-QTL regions and the genetic complexity of salt tolerance. The meta-QTLs identified in this study will be useful not only for MAS and pyramiding, but will also accelerate the fine mapping and cloning of candidate genes associated with salt-tolerance mechanisms in rice.


Euphytica ◽  
2014 ◽  
Vol 201 (3) ◽  
pp. 401-409 ◽  
Author(s):  
Wenqiang Liu ◽  
Tingting Lu ◽  
Yongchao Li ◽  
Xiaowu Pan ◽  
Yonghong Duan ◽  
...  

2019 ◽  
Vol 48 (D1) ◽  
pp. D856-D862 ◽  
Author(s):  
Wubin Ding ◽  
Jiwei Chen ◽  
Guoshuang Feng ◽  
Geng Chen ◽  
Jun Wu ◽  
...  

Abstract Aberrant DNA methylation plays an important role in cancer progression. However, no resource has been available that comprehensively provides DNA methylation-based diagnostic and prognostic models, expression–methylation quantitative trait loci (emQTL), pathway activity-methylation quantitative trait loci (pathway-meQTL), differentially variable and differentially methylated CpGs, and survival analysis, as well as functional epigenetic modules for different cancers. These provide valuable information for researchers to explore DNA methylation profiles from different aspects in cancer. To this end, we constructed a user-friendly database named DNA Methylation Interactive Visualization Database (DNMIVD), which comprehensively provides the following important resources: (i) diagnostic and prognostic models based on DNA methylation for multiple cancer types of The Cancer Genome Atlas (TCGA); (ii) meQTL, emQTL and pathway-meQTL for diverse cancers; (iii) Functional Epigenetic Modules (FEM) constructed from Protein-Protein Interactions (PPI) and Co-Occurrence and Mutual Exclusive (COME) network by integrating DNA methylation and gene expression data of TCGA cancers; (iv) differentially variable and differentially methylated CpGs and differentially methylated genes as well as related enhancer information; (v) correlations between methylation of gene promoter and corresponding gene expression and (vi) patient survival-associated CpGs and genes with different endpoints. DNMIVD is freely available at http://www.unimd.org/dnmivd/. We believe that DNMIVD can facilitate research of diverse cancers.


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