NUCLEAR-DNA CONTENT AND IN-VITRO INDUCED SOMATIC POLYPLOIDIZATION CASSAVA (MANIHOT-ESCULENTA CRANTZ) BREEDING

被引:61
作者
AWOLEYE, F
VANDUREN, M
DOLEZEL, J
NOVAK, FJ
机构
[1] INT ATOM ENERGY AGCY, JOINT FAO PROGRAMME, PLANT BREEDING UNIT, LAB SEIBERSDORF, A-1400 VIENNA, AUSTRIA
[2] ACAD SCI CZECH REPUBL, INST EXPTL BOT, DEPT PLANT BIOTECHNOL, CR-77200 OLOMOUC, CZECH REPUBLIC
关键词
FLOW CYTOMETRY; TETRAPLOIDY; MIXOPLOIDY; CASSAVA BREEDING; IN VITRO COLCHICINATION; ORYZALIN;
D O I
10.1007/BF00022164
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The diploid (2C) amount of DNA in cassava (Manihot esculenta Crantz) is 1.67 picograms (pg) per cell nucleus. This value corresponds to 772 mega-base pairs in the haploid genome. The size of the nuclear genome in cassava is very small in comparison with other Angiosperms. Flow cytometry techniques were used to screen ploidy levels in a large population of in vitro plantlets treated with colchicine and oryzalin (3,5-dinitro-N-4,N-dipropylsulphate). Culture of axillary node cuttings for 48 hours in liquid medium supplemented with 2.5 to 5.0 mM colchicine in combination with 2% dimethyl sulfoxide (DMSO) resulted in a high frequency (23 to 42%) of non-chimeric tetraploids in the V-3 generation. Although mixoploidy may persist in as many as four cycles of vegetative propagation of node cuttings, solid (non-chimeric) tetraploids can be identified by flow cytometry among in vitro plantlets and then rapidly propagated for field testing. A somatic polyploidization system is proposed for implementation in cassava breeding programmes.
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页码:195 / 202
页数:8
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