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| Authors: | J.H. Xie, W.H. Ma, C.M. Liu |
| Keywords: | genetic diversity, molecular marker, classification |
Abstract:
Thirty-two mango cultivars (Mangifera indica L.), including 13 Chinese, 9 USA, 4 Indian, 2 Australian, 2 Indonesian, 1 Thai and 1 Philippine cultivars, were examined using simple sequence repeat (SSRs) anchored primers. 15 primers gave reproducible DNA amplification patterns, and revealed a total number of 245 DNA bands, in which 215 bands were polymorphic; the percentage of polymorphic loci was 87.7%. The number of generated bands ranged from 6 to 26 per primer.
According to the band patterns obtained from these primers, all the cultivars could be distinguished from each other.
NTSY-2.0 software was used to calculate the Dice similarity coefficiency, and a dendrogram was constructed based on UPGMA cluster analysis.
The mango cultivars were divided into 5 groups.
The Indonesian cultivar ‘Arumanis’ was very far in genetic distance from the others and fell into a group by itself.
Nine USA and 2 Chinese cultivars with red skin were placed in a single group.
Nine Chinese, 2 Australian, 1 Thai and 1 Philippine cultivars belonged to a distinct group.
The others, including 4 Indian and 2 Chinese cultivars were scattered into two groups.
On the basis of these results and information on geographic origin, embryo-type, skin color and family structure, mango cultivars could be divided into five classes: I) Red skin type, generally originating from America or west, II) Indo-Chinese type, coming from southeast Asia, III) Southern Indian mango type, IV) Northern Indian mango type, and V) Indonesia type.
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