2013
DOI: 10.1007/s10142-013-0335-2
|View full text |Cite
|
Sign up to set email alerts
|

Sorghum bmr6 mutant analysis demonstrates that a shared MYB1 transcription factor binding site in the promoter links the expression of genes in related pathways

Abstract: Sorghum is not only an important cereal crop but also a biofuel crop. The sorghum brown midrib mutant 6 (bmr6) has a reduced lignin content in the cell walls and vascular tissues, which could potentially be advantageous for cellulosic biofuel production. Meanwhile, both dry matter yield and plant height were decreased in the bmr6 mutant. To identify genes affected in the mutant, differential gene expression analysis was performed for bmr6 and the wild type. As a result, a total of 1,052 differentially expresse… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
8
0
1

Year Published

2014
2014
2023
2023

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 10 publications
(9 citation statements)
references
References 34 publications
0
8
0
1
Order By: Relevance
“…Until now, sorghum qPCR assays were performed using a single reference gene to quantify target gene expression in response to various experimental conditions. Traditional reference genes including 18S RNA, Actin, EIF4 α, Tubulin , and Ubiquitin have been used as calibrators for quantifying sorghum gene expression in response to abiotic stresses and during plant growth and development (Yang et al, 2004 ; Jain et al, 2008 ; Cook et al, 2010 ; Shen et al, 2010 ; Wang et al, 2010 ; Dugas et al, 2011 ; Ishikawa et al, 2011 ; Koegel et al, 2013 ; Li et al, 2013 ; Gelli et al, 2014 ; Shakoor et al, 2014 ; Yang et al, 2014b ; Yin et al, 2014 ; Kebrom and Mullet, 2015 ; Li et al, 2015 ; Walder et al, 2015 ). Nevertheless, the reference genes used in these studies were randomly selected from various sources without any experimental validation.…”
Section: Introductionmentioning
confidence: 99%
“…Until now, sorghum qPCR assays were performed using a single reference gene to quantify target gene expression in response to various experimental conditions. Traditional reference genes including 18S RNA, Actin, EIF4 α, Tubulin , and Ubiquitin have been used as calibrators for quantifying sorghum gene expression in response to abiotic stresses and during plant growth and development (Yang et al, 2004 ; Jain et al, 2008 ; Cook et al, 2010 ; Shen et al, 2010 ; Wang et al, 2010 ; Dugas et al, 2011 ; Ishikawa et al, 2011 ; Koegel et al, 2013 ; Li et al, 2013 ; Gelli et al, 2014 ; Shakoor et al, 2014 ; Yang et al, 2014b ; Yin et al, 2014 ; Kebrom and Mullet, 2015 ; Li et al, 2015 ; Walder et al, 2015 ). Nevertheless, the reference genes used in these studies were randomly selected from various sources without any experimental validation.…”
Section: Introductionmentioning
confidence: 99%
“…According to the relative positions of the markers on the reference sorghum genome (www.gramene.org), a search was performed for candidate genes involved in cellulose and lignin biosynthesis (Li et al, 2013). A gene that is similar to glycosyltransferase (Sb03g026550) in conjugating lignin monomers was found close to qADF3 and qNDF3 on chromosome 3.…”
Section: Discussionmentioning
confidence: 99%
“…Raw sequences were transformed into clean tags by filtering off adapter-only tags and low-quality tags as described (Li et al, 2013). All the clean tags were mapped to the reference sequences of Sorghum bicolor and only 1 bp of mismatch was considered.…”
Section: Sequence Annotation and Dges Pathways Identificationmentioning
confidence: 99%