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Journal ArticleDOI

Identification of restriction fragment length polymorphism and random amplified polymorphic DNA markers linked to downy mildew resistance genes in lettuce, using near-isogenic lines.

Ilan Paran, +2 more
- 01 Dec 1991 - 
- Vol. 34, Iss: 6, pp 1021-1027
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TLDR
The rapid screening and identification of tightly linked markers to the target genes demonstrated the potential of RAPD markers for saturating genetic maps.
Abstract
Near-isogenic lines were used to identify restriction fragment length polymorphism (RFLP) and random amplified polymorphic DNA (RAPD) markers linked to genes for resistance to downy mildew (Dm) in lettuce. Two pairs of near-isogenic lines that differed for Dm1 plus Dm3 and one pair of near-isogenic lines that differed for Dm11 were used as sources of DNA. Over 500 cDNAs and 212 arbitrary 10-mer oligonucleotide primers were screened for their ability to detect polymorphism between the near-isogenic lines. Four RFLP markers and four RAPD markers were identified as linked to the Dm1 and Dm3 region. Dm1 and Dm3 are members of a cluster of seven Dm genes. Marker CL922 was absolutely linked to Dm15 and Dm16, which are part of this cluster. Six RAPD markers were identified as linked to the Dm11 region. The use of RAPD markers allowed us to increase the density of markers in the two Dm regions in a short time. These regions were previously only sparsely populated with RFLP markers. The rapid screening and identification of tightly linked markers to the target genes demonstrated the potential of RAPD markers for saturating genetic maps.

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Citations
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Journal ArticleDOI

Development of reliable PCR-based markers linked to downy mildew resistance genes in lettuce

TL;DR: Sequence characterized amplified regions (SCARs) were derived from eight random amplified polymorphic DNA (RAPD) markers linked to disease resistance genes in lettuce, providing information on the molecular basis of RAPD markers.
Journal ArticleDOI

Applications of random amplified polymorphic DNA (RAPD) in molecular ecology

TL;DR: The Random Amplified Polymorphic DNA (RAPD) technique may be used in molecular ecology to determine taxonomic identity, assess kinship relationships, analyse mixed genome samples, and create specific probes.
Journal ArticleDOI

Advances in molecular marker techniques and their applications in plant sciences

TL;DR: A new class of advanced marker techniques has emerged, primarily derived from combination of earlier basic techniques, thereby revealing genetic variation through increased genome coverage.
Journal ArticleDOI

Reproducibility of random amplified polymorphic DNA (RAPD) analysis among laboratories

TL;DR: Random amplified polymorphic DNA (RAPD) analysis appears to offer a cost- and time-effective alternative to restriction fragment-length polymorphism (RFLP) analysis, but concerns about the ability to compare RAPD results from one laboratory to another have not been addressed effectively.
References
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Journal ArticleDOI

MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations

TL;DR: A computer package, called MAPMAKER, designed specifically for the construction of linkage maps in a number of organisms, including the human and several plants, and it is outlined the mapping strategies that have been used.
Journal ArticleDOI

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

TL;DR: YTOGENETIC analysis has identified chromosome Ilpl3 as the smallest overlap region for deletions found in individuals with WAGR syndrome, which includes Wilms tumour, anirida, genito-urinary abnormalities and mental retardation.
Journal ArticleDOI

Applications of random amplified polymorphic DNA (RAPD) in molecular ecology

TL;DR: The Random Amplified Polymorphic DNA (RAPD) technique may be used in molecular ecology to determine taxonomic identity, assess kinship relationships, analyse mixed genome samples, and create specific probes.
Book ChapterDOI

DNA Markers in Plant Improvement

TL;DR: This chapter addresses the applications of DNA markers to plant breeding, allowing researchers to begin to tap the potential of this technology to the benefit of both basic biology and agricultural productivity.
Journal ArticleDOI

Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction.

TL;DR: An approach for screening ordered arrays of yeast artificial-chromosome (YAC) clones containing human DNA that is based on the polymerase chain reaction (PCR), allowing the identification and isolation of numerous YAC clones containing specific human genes.
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