Plant Molecular Biology 2 1991
DOI: 10.1007/978-1-4615-3304-7_26
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Application of Restriction Fragment Length Polymorphism to Maize Breeding

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Cited by 4 publications
(4 citation statements)
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“…The presence of duplicated genes in maize has been observed for loci controlling morphological traits (26), isozyme loci (27), and RFLP loci (28,29). The mechanism by which these duplications originated is not known, but mapping experiments with RFLP loci have indicated that they are usually duplicated on separate chromosomes and that large segments of different chromosomes sometimes contain these duplicated loci in the same linear order.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The presence of duplicated genes in maize has been observed for loci controlling morphological traits (26), isozyme loci (27), and RFLP loci (28,29). The mechanism by which these duplications originated is not known, but mapping experiments with RFLP loci have indicated that they are usually duplicated on separate chromosomes and that large segments of different chromosomes sometimes contain these duplicated loci in the same linear order.…”
Section: Discussionmentioning
confidence: 99%
“…Similarly, two maize chromosome VII locus probes identified a pair of linked loci in a linkage group composed of mostly maize chromosome II probes. Chromosomes III and VIII of maize commonly share duplicated loci as do chromosomes II and VII (28,29).…”
Section: Discussionmentioning
confidence: 99%
“…tomato mosaic virus resistance (YOUNG et al 1988), Bremia lactuca resistance (KESSELI et al 1991), rice blast resistance (Yu et al 1991) or powdery mildew {Erysiphe graminis) resistance (ScHULLER et al 1992). Markers tightly linked to a target gene are expected considerably to reduce the number of generations necessary to introduce a new gene via backcross breeding procedures (TANKSLEY et al 1989, MURRAY et al 1991.…”
mentioning
confidence: 99%
“…Examples include genes isolated by transposon tagging or by messenger selection and reverse transcription to produce a defined eDNA. In contrast, the agr probes developed and mapped by Murray et al ( 1989) are random cDNAs from tissue-specific libraries, which have been mapped with bnl and umc RFLP markers. Substantial numbers of random eDNA clones have been sequenced (Keith et al, 1993) and loci for them are being mapped (Chao et al, 1994;Personal Communication, Maize Genet.…”
Section: Genomes Of Maize and Sorghummentioning
confidence: 99%