Articles
Identification of S-genotypes in local pear cultivars from the Yellow River area
Article number
1401_8
Pages
53 – 60
Language
English
Abstract
There are many endemic pear germplasm resources distributed in the ancient Yellow River area.
Identification of pear S-genotype is an important basis for pear breeding and production.
Using a pair of consensus primers specific to pear S-RNase, PCR amplification from genomic DNA of 17 local cultivars were carried out.
Then the PCR products were purified and sequenced.
The PCR amplification results showed that all cultivars contained two S-RNase fragment bands.
Dangshansuli, Dangshanxinsu, Dangshanfusu, Dangshanxisu, Zipicao, Qingpicao, Fusu, Hanli, Xiangmianli, Heli, Wanli No.2, Wanli No.5 and Wanli No.6, these 13 cultivars all contained two common bands, one identified as S34-RNase (DQ269500), another fragment sequence have 100% homology with S7-RNase (AB002143) and S27-RNase (EF643640) sequences in GenBank.
Based on the analysis of the S-gene, it was confirmed that S7-RNase and S27-RNase exon amino acid sequences are identical.
Therefore, the S-genotypes of Dangshansuli, Hanli, Xiangmianli, Dangshanfusu, Qingpicao, Jizaosu, Heli, Lianglizaosu, Dangshanxinsu, Wanli 4, Wanli 6 and Dangshanxisu, were identified as S7 S34 or S27 S34. The other five pear cultivars were identified as, Shuihulu (S19S34), Waiweibacao (S1S19), Jizhuahuang (S1S34), Wanli 5 (S3S34), Zisu (S19S34), Jizhuahuang (S1S34). Through the identification of the S-genotypes, out of 17 cultivars, there are 16 cultivars tested contained S34-RNase. This implies that S34-RNase is the dominant S-RNase of pears in the ancient Yellow River region.
Identification of pear S-genotype is an important basis for pear breeding and production.
Using a pair of consensus primers specific to pear S-RNase, PCR amplification from genomic DNA of 17 local cultivars were carried out.
Then the PCR products were purified and sequenced.
The PCR amplification results showed that all cultivars contained two S-RNase fragment bands.
Dangshansuli, Dangshanxinsu, Dangshanfusu, Dangshanxisu, Zipicao, Qingpicao, Fusu, Hanli, Xiangmianli, Heli, Wanli No.2, Wanli No.5 and Wanli No.6, these 13 cultivars all contained two common bands, one identified as S34-RNase (DQ269500), another fragment sequence have 100% homology with S7-RNase (AB002143) and S27-RNase (EF643640) sequences in GenBank.
Based on the analysis of the S-gene, it was confirmed that S7-RNase and S27-RNase exon amino acid sequences are identical.
Therefore, the S-genotypes of Dangshansuli, Hanli, Xiangmianli, Dangshanfusu, Qingpicao, Jizaosu, Heli, Lianglizaosu, Dangshanxinsu, Wanli 4, Wanli 6 and Dangshanxisu, were identified as S7 S34 or S27 S34. The other five pear cultivars were identified as, Shuihulu (S19S34), Waiweibacao (S1S19), Jizhuahuang (S1S34), Wanli 5 (S3S34), Zisu (S19S34), Jizhuahuang (S1S34). Through the identification of the S-genotypes, out of 17 cultivars, there are 16 cultivars tested contained S34-RNase. This implies that S34-RNase is the dominant S-RNase of pears in the ancient Yellow River region.
Authors
Yongjie Qi, Na Ma, LiQing Lu, Fanjun Ke, Liping Kan, Zixian Zha, Yiliu Xu, Zhenghui Gao
Keywords
S-genotype, local pear resources, ancient Yellow River area
Online Articles (40)
