2006
DOI: 10.1016/j.pmpp.2006.07.002
|View full text |Cite
|
Sign up to set email alerts
|

Differential gene expression in loblolly pine (Pinus taeda L.) challenged with the fusiform rust fungus, Cronartium quercuum f.sp. fusiforme

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
17
0

Year Published

2007
2007
2022
2022

Publication Types

Select...
6
2

Relationship

2
6

Authors

Journals

citations
Cited by 22 publications
(17 citation statements)
references
References 22 publications
0
17
0
Order By: Relevance
“…Given this rapid progress, it seems reasonable to conclude that much of the improvement has been due to selection for major gene resistance [3,[30][31][32]. Genomic markers now enable detection of parents that harbor specific Fr genes, so that their progeny deployed in plantation forests can be monitored for durability under field conditions.…”
Section: Discussionmentioning
confidence: 99%
“…Given this rapid progress, it seems reasonable to conclude that much of the improvement has been due to selection for major gene resistance [3,[30][31][32]. Genomic markers now enable detection of parents that harbor specific Fr genes, so that their progeny deployed in plantation forests can be monitored for durability under field conditions.…”
Section: Discussionmentioning
confidence: 99%
“…For our marker work, we relied primarily on random amplified polymorphic DNA (RAPD) markers that were used in all matrix families. RAPD protocols underwent multiple minor modifications over the many years of this work, but refer to Myburg et al [31] for the most recently optimized protocols. Amplified fragment length polymorphism (AFLP) markers were utilized for only a single family × isolate combination.…”
Section: Fr Gene Mappingmentioning
confidence: 99%
“…In tree 10-005, the + (band present) allele of marker J7_470 and the − (band absent) allele of marker AJ4_420 are coupled with each other and the Fr1 resistance allele, while −J7_470 and +AJ4_420 are coupled with each other and the fr1 non-resistance allele (H. Amerson, unpublished data, cited in Myburg et al 2006). Since RAPD markers are dominant markers, it was necessary that one and, preferably, both markers (J7_470, AJ4_420) be homozygous null (uniformly band absent in the slash female) if one or both of the markers were to be successfully used to make allele calls (Fr1 vs. fr1 inherited from the loblolly parent) in the hybrid progeny.…”
Section: Genetic Marker Background and Preliminary Studiesmentioning
confidence: 99%
“…Haploid and diploid samples were treated the same except that RAPD reactions for haploid samples utilized 5 ng of template DNA, while those for diploid samples utilized 7.5 ng of template DNA. RAPD reactions (with noted haploid vs. diploid template differences), PCR conditions/specifications, gel electrophoresis, DNA band visualization, and recording (for our study markers) all followed the protocol of Myburg et al (2006). Markers J7_470 and AJ4_420 were scored as band present vs. absent by visual assessment.…”
Section: Dna Isolation and Rapd Marker Protocolsmentioning
confidence: 99%