2014
DOI: 10.1155/2014/296020
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Biogeographical Variation and Population Genetic Structure ofSporisorium scitamineumin Mainland China: Insights from ISSR and SP-SRAP Markers

Abstract: A total of 100 Sporisorium scitamineum isolates were investigated by inter simple sequence repeat (ISSR) and single primer-sequence related amplified polymorphism (SP-SRAP) markers. These isolates were clearly assorted into three distinct clusters regardless of method used: either cluster analysis or by principal component analysis (PCA) of the ISSR, SP-SRAP, or ISSR + SP-SRAP data set. The total gene diversity (H t) and gene diversity between subpopulations (H s) were estimated to be 0.34 to 0.38 and 0.22 to … Show more

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Cited by 12 publications
(21 citation statements)
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“…Molecular detection of the smut pathogen in sugarcane has become possible by using polymerase chain reaction (PCR) to amplify the bE mating-type gene of S. scitamineum (Byther and Steiner, 1974;Albert and Schenck, 1996;Schenck, 1998;Singh et al, 2004;Su et al, 2013). Random-amplified polymorphic DNA, amplified fragment length polymorphism, sequence-related amplified polymorphism, inter-simple sequence repeat, and internal transcribed spacer (ITS) sequence analysis have been used to evaluate intraspecies diversity within S. scitamineum isolates (Victoria et al, 1997;Bakkeren et al, 2000;Braithwaite et al, 2004;Stoll et al, 2003Stoll et al, , 2005Xu et al, 2004Xu et al, , 2014Singh et al, 2005;Baraket et al, 2009;Que et al, 2012Que et al, , 2014a. Therefore, molecular methods can be applied for phylogeny analysis because the phylogeny of S. scitamineum is poorly understood.…”
Section: Introductionmentioning
confidence: 99%
“…Molecular detection of the smut pathogen in sugarcane has become possible by using polymerase chain reaction (PCR) to amplify the bE mating-type gene of S. scitamineum (Byther and Steiner, 1974;Albert and Schenck, 1996;Schenck, 1998;Singh et al, 2004;Su et al, 2013). Random-amplified polymorphic DNA, amplified fragment length polymorphism, sequence-related amplified polymorphism, inter-simple sequence repeat, and internal transcribed spacer (ITS) sequence analysis have been used to evaluate intraspecies diversity within S. scitamineum isolates (Victoria et al, 1997;Bakkeren et al, 2000;Braithwaite et al, 2004;Stoll et al, 2003Stoll et al, , 2005Xu et al, 2004Xu et al, , 2014Singh et al, 2005;Baraket et al, 2009;Que et al, 2012Que et al, , 2014a. Therefore, molecular methods can be applied for phylogeny analysis because the phylogeny of S. scitamineum is poorly understood.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, this report also showed that the American and African populations all belonged to a single lineage which was also found among some Asian populations. Previous studies (Que et al, 2012;Shen et al, 2012a;Xu et al, 2014) on genetic diversity of S. scitamineum collected from China showed that the molecular diversity of S. scitamineum was associated with its geographical origin. Shen et al (2012a) also suggested that majority of S. scitamineum in sugarcane-producing regions of Southern China may belong to or are genetically similar to race 3.…”
Section: Introductionmentioning
confidence: 98%
“…The disease has caused serious problems in sugarcane plantation and sugar production, especially in the last 15 years due to the susceptibility of the sugarcane cultivar ROC22 which occupies more than 50% of the total sugarcane planting area in China. The average of smut infection rate in ROC22 is over 8% in plant cane and 15% in ratoon cane, respectively (Shen et al, 2013;Xu et al, 2014). The disease has now caused the most serious economic loss of sugarcane in China.…”
Section: Introductionmentioning
confidence: 99%
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