1998
DOI: 10.1016/s0958-1669(98)80119-5
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Gene discovery for crop improvement

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Cited by 18 publications
(8 citation statements)
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“…However, the success of map-based cloning mainly depends on: (i) an accurately segregating population of the target trait, (ii) availability of a large number of DNA markers and feasibility of their application, (iii) availability of suitable genomic libraries and/or nucleotide sequence information corresponding to the candidate genomic region and (iv) efficient transformation and evaluation systems of transgenic plants. The importance of these factors has been reviewed by Tanksley, Ganal, & Martin (1995) and by Martin (1998). In spite of improvements in the cloning of genes on the basis of phenotype, even a skilled scientist can take some time to use a mutant to identify the affected gene.…”
Section: A Use Of Forward and Reverse Genetics And Transgenic Approamentioning
confidence: 99%
“…However, the success of map-based cloning mainly depends on: (i) an accurately segregating population of the target trait, (ii) availability of a large number of DNA markers and feasibility of their application, (iii) availability of suitable genomic libraries and/or nucleotide sequence information corresponding to the candidate genomic region and (iv) efficient transformation and evaluation systems of transgenic plants. The importance of these factors has been reviewed by Tanksley, Ganal, & Martin (1995) and by Martin (1998). In spite of improvements in the cloning of genes on the basis of phenotype, even a skilled scientist can take some time to use a mutant to identify the affected gene.…”
Section: A Use Of Forward and Reverse Genetics And Transgenic Approamentioning
confidence: 99%
“…Molecular marker technologies have led to the rapid development of detailed genetic maps for many crop plants (Martin, 1998). Genetic linkage maps provide a framework for studying simple and complex traits.…”
mentioning
confidence: 99%
“…Then, the size of the population for segregation should be increased to narrow the locus with new polymorphic markers such as SSR, or newly designed PCR primers using genome sequence information. Finally, the target region will be revealed within less than 30 kb and the candidate genes must appear (Tanksley et al 1995, Martin 1998. The main problems with this approach are as follows: 1) dependence of recombination probability on precise tagging; 2) availability of only Nipponbare genome sequences; and 3) final identification of the candidate genes relies solely on the transformation or multiple alleles, if present.…”
Section: Actual Identification Of Genes Corresponding To Traitsmentioning
confidence: 99%