Inheritance of leaf color and sequence-related amplified polymorphic (SRAP) molecular markers linked to the leaf color gene in Brassica juncea

2011 ◽  
Vol 10 (66) ◽  
Author(s):  
Luo
2009 ◽  
Vol 25 (1) ◽  
pp. 57-65 ◽  
Author(s):  
Aixia Xu ◽  
Zhen Huang ◽  
Chaozhi Ma ◽  
Enshi Xiao ◽  
Guangwen Tian ◽  
...  

PLoS ONE ◽  
2016 ◽  
Vol 11 (4) ◽  
pp. e0153962 ◽  
Author(s):  
Haiying Guan ◽  
Xiangbo Xu ◽  
Chunmei He ◽  
Chunxiao Liu ◽  
Qiang Liu ◽  
...  

Pedosphere ◽  
2020 ◽  
Vol 30 (4) ◽  
pp. 517-527 ◽  
Author(s):  
Afsana PRAVEEN ◽  
Chandana PANDEY ◽  
Ehasanullah KHAN ◽  
Medha PANTHRI ◽  
Meetu GUPTA

Author(s):  
Muhammad Zailani ◽  
Retno Astuti Kuswardani ◽  
Ellen L. Panggabean

This study aims to determine the Response Growth and Production of Crops (Brassica juncea L.) Against Watering Time Interval In Various Hydroponics Media. The research was conducted at the experimental gardens of Faculty of Agriculture, Faculty of Agriculture, University of Medan Area, located on No. Pond Street. 1 Medan Estate. This research was conducted from October 2013 until December 2013. The design used was RAL Factorial, with 2 replications, 10 combinations. The first factor of the hydroponic planting medium is: M1: Frying Roots, M2: Coconut Coir Powder, M3: Fryer Seal, M4: Rokwool, and M5: Sawdust, the second factor is the time interval: I1: 3 hours a day I2: 5 hours a day, starting from 08:00 a.m to 06:00 p.m. The result of this research indicates that the treatment of watering liquid fertilizer with different time interval does not show a real effect on the growth of mustard plants, Media treatment used on hydroponic systems have an influence very evident on the parameters of plant height, leaf number, leaf area, production weight and significant effect on leaf level parameters, influential planting medium and have the best number is M3 (fuel husk). Interaction interval of watering time on various hydroponic media did not have a significant effect on observed parameters, namely: plant height, leaf number, wet weight, and weight of production, while the leaf color parameter had significant effect on leaf width.


2013 ◽  
Vol 33 (2) ◽  
pp. 425-434 ◽  
Author(s):  
Ping Xu ◽  
Zewen Lv ◽  
Xiangxiang Zhang ◽  
Xiaohua Wang ◽  
Yuanyuan Pu ◽  
...  

Euphytica ◽  
2005 ◽  
Vol 144 (1-2) ◽  
pp. 157-167 ◽  
Author(s):  
Tariq Mahmood ◽  
Muhammad H. Rahman ◽  
Gary R. Stringam ◽  
Francis Yeh ◽  
Allen Good

PLoS ONE ◽  
2014 ◽  
Vol 9 (6) ◽  
pp. e99564 ◽  
Author(s):  
Xiao-juan Deng ◽  
Hai-qing Zhang ◽  
Yue Wang ◽  
Feng He ◽  
Jin-ling Liu ◽  
...  

2015 ◽  
Vol 95 (5) ◽  
pp. 939-945 ◽  
Author(s):  
Binay K. Singh ◽  
Divakar Nandan ◽  
Supriya Ambawat ◽  
Bhagirath Ram ◽  
Arun Kumar ◽  
...  

Singh, B. K., Nandan, D., Supriya, A., Ram, B., Kumar, A., Singh, T., Meena, H. S., Kumar, V., Singh, V. V., Rai, P. K. and Singh, D. 2015. Validation of molecular markers for marker-assisted pyramiding of white rust resistance loci in Indian Mustard (Brassica juncea L.). Can. J. Plant Sci. 95: 939–945. Successful application of molecular markers in marker-assisted pyramiding relies on effective determination of the target phenotype. In this respect, evaluation of the efficiency of markers for marker-assisted selection through cross-validation in different genetic backgrounds and in different populations is a crucial step. In the present study, the previously identified Arabidopsis-derived intron polymorphic (IP) markers At5g41560 and At2g36360, which were highly linked with AcB1-A4.1 and AcB1-A5.1, respectively, were validated in a set of 25 genotypes of Indian Mustard and in three different F2 populations. The relationships between the variation of PCR products of the two markers with the percent disease index (PDI) of the tested genotypes, and the co-segregation analysis of the markers with disease phenotype in F2 populations clearly indicated that At5g41560 and At2g36360 are genotype-nonspecific markers and are closely linked to white rust resistance loci AcB1-A4.1 and AcB1-A5.1, respectively. It also became evident from the present study that AcB1-A4.1 and an another white rust resistance locus Ac(2)t are likely the same gene locus.


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