scholarly journals The efficiency of interaction between cytokines and Auxins in Micropropagation of Chrysanthemum plant (Chrysanthemum indicum L.)

2021 ◽  
Vol 735 (1) ◽  
pp. 012048
Author(s):  
Abdulwadood S.M. Alsoufi ◽  
Ziyad Shihab Ahmed ◽  
Aysar M. Salim
2011 ◽  
Vol 1 (9) ◽  
pp. 7-10
Author(s):  
M.Jerome Rozario ◽  
◽  
Dr.A.John Merina ◽  
Dr.V.Srinivasana Dr.V.Srinivasana

2009 ◽  
Vol 38 (10) ◽  
pp. 1406-1413 ◽  
Author(s):  
Sang-Hoon Lee ◽  
In-Guk Hwang ◽  
Ha-Kyoo Lee ◽  
So-Lim Shin ◽  
Young-Deug Chang ◽  
...  

2010 ◽  
Vol 7 (12) ◽  
pp. 2951-2962 ◽  
Author(s):  
Cong Zhang ◽  
Min-Jian Qin ◽  
Pan Shu ◽  
Jun-Li Hong ◽  
Lin Lü ◽  
...  

PeerJ ◽  
2017 ◽  
Vol 5 ◽  
pp. e2933 ◽  
Author(s):  
Hoseong Choi ◽  
Yeonhwa Jo ◽  
Ju-Yeon Yoon ◽  
Seung-Kook Choi ◽  
Won Kyong Cho

Viroids are the smallest infectious agents, and their genomes consist of a short single strand of RNA that does not encode any protein.Chrysanthemum stunt viroid(CSVd), a member of the familyPospiviroidae, causes chrysanthemum stunt disease. Here, we report the genomic variations of CSVd to understand the sequence variability of CSVd in different chrysanthemum cultivars. We randomly sampled 36 different chrysanthemum cultivars and examined the infection of CSVd in each cultivar by reverse transcription polymerase chain reaction (RT-PCR). Eleven cultivars were infected by CSVd. Cloning followed by Sanger sequencing successfully identified a total of 271 CSVd genomes derived from 12 plants from 11 cultivars. They were further classified into 105 CSVd variants. Each single chrysanthemum plant had a different set of CSVd variants. Moreover, different single plants from the same cultivar had different sets of CSVd variants but identical consensus genome sequences. A phylogenetic tree using 12 consensus genome sequences revealed three groups of CSVd genomes, while six different groups were defined by the phylogenetic analysis using 105 variants. Based on the consensus CSVd genome, by combining all variant sequences, we identified 99 single-nucleotide variations (SNVs) as well as three nucleotide positions showing high mutation rates. Although 99 SNVs were identified, most CSVd genomes in this study were derived from variant 1, which is identical to known CSVd SK1 showing pathogenicity.


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