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   <subfield code="a">Production and molecular characterization of potential seedless cybrid plants between pollen sterile Satsuma mandarin and two seedy Citrus cultivars</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Xiao-Dong Cai, Jing Fu, Xiu-Xin Deng, Wen-Wu Guo]</subfield>
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   <subfield code="a">Cytoplasmic male sterility (CMS) is known to be controlled by mitochondrial genome in higher plants including Satsuma mandarin (Citrus unshiu Marc.). Citrus symmetric fusion experiments often produce diploid cybrids possessing nuclear DNA from the mesophyll parent and mitochondrial DNA (mtDNA) from the embryogenic callus parent. Therefore, it is possible to transfer CMS from Satsuma mandarin as callus parent to seedy citrus cultivars as leaf one by somatic cybridization. Herein, symmetric fusion technique was adopted to create cybrids for potential seedlessness by transferring CMS from Citrus unshiu Marc. cv. Guoqing No. 1 (G1) to two traditional Chinese seedy citrus cultivars, ‘Shatian' pummelo (C. grandis (L) Osbeck) and ‘Bingtang' orange (C. sinensis (L) Osbeck). Flow cytometry analysis showed that 19 plants recovered from G1+‘Bingtang' orange and 17 of 35 plants regenerated from G1+‘Shatian' pummelo were diploid. The remaining plants from G1+‘Shatian' pummelo were tetraploid. The diploid plants from the two combinations were confirmed as true cybrids by simple sequence repeat (SSR) and cleaved amplified polymorphic sequence (CAPS) analysis, with nuclear DNA from their corresponding leaf parent and mtDNA from their common suspension parent, G1 Satsuma mandarin. The remaining plants from G1+‘Shatian' pummelo were identified as somatic hybrids with mtDNA from G1. The chloroplast simple sequence repeat (cp-SSR) analysis revealed somatic hybrid/cybrid plants from the two combinations in most cases possessed either of their parental chloroplast type, and two plants from G1+‘Shatian' pummelo and all embryoids analyzed from G1+‘Bingtang' orange possessed chloroplast DNA (cpDNA) from both parents. These results demonstrated that we succeeded in introducing mtDNA from G1 Satsuma mandarin into the two target seedy citrus cultivars for potential seedlessness through symmetric fusion.</subfield>
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   <subfield code="a">Springer Science+Business Media B.V., 2007</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Citrus</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Cybrids</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Cytoplasmic male sterility</subfield>
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   <subfield code="a">Molecular analysis</subfield>
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   <subfield code="a">Seedlessness</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Somatic hybridization</subfield>
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   <subfield code="a">CAPS : Cleaved amplified polymorphic sequence</subfield>
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   <subfield code="a">CpDNA : Chloroplast DNA</subfield>
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   <subfield code="a">cp-SSR : Chloroplast simple sequence repeat</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">G1 : Satsuma mandarin, Citrus unshiu Marc. cv. Guoqing No. 1</subfield>
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   <subfield code="a">SSR : Simple sequence repeat</subfield>
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   <subfield code="a">MtDNA : Mitochondrial DNA</subfield>
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   <subfield code="a">MT : Murashige and Tucker (1969)</subfield>
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   <subfield code="u">National Key Laboratory of Crop Genetic Improvement, National Center of Crop Molecular Breeding, Huazhong Agricultural University, 430070, Wuhan, China</subfield>
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   <subfield code="t">Plant Cell, Tissue and Organ Culture</subfield>
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   <subfield code="g">90/3(2007-09-01), 275-283</subfield>
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