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   <subfield code="a">10.1007/s001220051376</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s001220051376</subfield>
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   <subfield code="a">A genetic map of the Nicotiana alata S locus that includes three pollen-expressed genes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[J.-H. Li, N. Nass, M. Kusaba, P. N. Dodds, N. Treloar, A. E. Clarke, E. Newbigin]</subfield>
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   <subfield code="a">Abstract : The S locus of solanaceous plants includes separate genes that control the self-incompatibility phenotype of the pistil and of the pollen. The gene controlling the self-incompatibility phenotype of the pistil encodes an extracellular ribonuclease, the S-RNase. The gene(s) controlling the self-incompatibility phenotype of pollen (the pollen-S gene) has yet to be identified. As part of a long-term strategy to clone the pollen-S gene by chromosome walking, a detailed map of the region near the S locus of Nicotiana alata was generated using a total of 251 F2 plants. The map spans an interval of approximately 2.6 cM and contains five markers as well as the S-RNase gene. Two markers were detected with heterologous probes that also detect sequences linked to the S locus of Solanum tuberosum and the homologous region of the Lycopersicon genome. Three markers were identified by differential display using N. alata pollen RNA as a template. One of these markers is a pollen-expressed sequence, 48A, which detects a polymorphic marker no more than 0.5 cM from the S locus. RNA blot analysis indicates that the 48A gene is expressed primarily during pollen development after the completion of meiosis and is therefore a candidate for the pollen-S gene. The utility of these markers and the possible involvement of 48A in the molecular mechanism of self- incompatibility are discussed.</subfield>
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   <subfield code="a">Springer-Verlag Berlin Heidelberg, 2000</subfield>
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   <subfield code="a">Key words Gametophytic self-incompatibility</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">S locus</subfield>
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   <subfield code="a">Differential display</subfield>
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   <subfield code="a">Pollen-expressed genes</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Restriction fragment length polymorphisms (RFLPs)</subfield>
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   <subfield code="a">Li</subfield>
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   <subfield code="u">Plant Cell Biology Research Centre, School of Botany, The University of Melbourne, del Parkville, Victoria, 3010 Australia e-mail: e.newbigin@botany.unimelb.edu,au; Fax: +613-9347-1071, AU</subfield>
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   <subfield code="a">Nass</subfield>
   <subfield code="D">N.</subfield>
   <subfield code="u">Institute for Plant Biochemistry, Weinberg 3, D-06120 Halle (Saale), Germany, DE</subfield>
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   <subfield code="a">Kusaba</subfield>
   <subfield code="D">M.</subfield>
   <subfield code="u">Institute of Radiation Breeding, National Institute of Agrobiological Resources, Ministry of Agriculture, Forestry and Fisheries, Ohmiya Naka-gun, Ibaraki 319-22, Japan, JP</subfield>
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   <subfield code="u">Commonwealth Scientific and Industrial Research Organization, Plant Industry, GPO Box 1600, Canberra, ACT 2601, Austrialia, AT</subfield>
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   <subfield code="u">Plant Cell Biology Research Centre, School of Botany, The University of Melbourne, del Parkville, Victoria, 3010 Australia e-mail: e.newbigin@botany.unimelb.edu,au; Fax: +613-9347-1071, AU</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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