Kim Hoy-Taek, Hirata Yutaka, Nou Ill-Sup
Faculty of Plant Science and Production, Sunchon National University, Korea.
Mol Cells. 2002 Jun 30;13(3):444-51.
The pear (Pyrus pyrifolia) has gametophytic self-incompatibility (GSI). To elucidate the S-genotypes of Korean-bred pear cultivars, whose parents are heterozygotes, the PCR amplification using S-RNase primers that are specific for each S-genotype was carried out in 15 Korean-bred pear cultivars and 5 Japanese-bred pear cultivars. The difference of the fragment length was shown in the following order: S6 (355 bp) < S7 (360 bp) < S1 (375 bp) < S4 (376 bp) < S3 and S5 (384 bp) < S8 (442 bp) < S9 (1,323 bp) < S2 (1,355 bp). We analyzed the sequence of the S-RNase gene, which had introns of various sizes in the hypervariable (HV) region between the adjacent exons with a fairly high homology. The sizes of the introns were as follows: S1 = 167 bp, S2 = 1,153 bp, S3 = 179 bp, S4 = 168 bp, S5 = 179 bp, S6 = 147 bp, S7 = 152 bp, S8 = 234 bp, S9 = 1,115 bp. There were five conservative and five hypervariable regions in the introns of S1, S3, S4, S5, S6 and S-RNases. A pairwise comparison of these introns of S-RNases revealed homologies as follows: 93.7% between S1- and S4-RNases, 93.3% between S3- and S5-RNases and 78.9% between S6- and S7-RNases. PCR-RFLP and S-RNases sequencing determined the S-genotypes of the pear cultivars. The S-genotypes were S4S9 for Shinkou, S3S9 for Niitaka, S3S5 for Housui, S1S5 for Kimizukawase, S1S8 for Ichiharawase, S3S5 for Mansoo, S3S4 for Shinil, S3S4 for Whangkeumbae, S3S5 for Sunhwang, S3S5 for Whasan, S3S5 for Mihwang, S5S? for Chengsilri, S3S5 for Gamro, S3S4 for Yeongsanbae, S3S4 for Wonhwang, S3S5 for Gamcheonbae, S3S5 for Danbae, S3S4 for Manpoong, S3S4 for Soowhangbae and S4S6 for Chuwhangbae. The information on the S-genotypes of pear cultivars will be used for the pollinizer selection and breeding program.
梨(Pyrus pyrifolia)具有配子体自交不亲和性(GSI)。为了阐明韩国培育的梨品种(其亲本为杂合子)的S基因型,使用针对每种S基因型的S-RNase引物对15个韩国培育的梨品种和5个日本培育的梨品种进行了PCR扩增。片段长度差异如下:S6(355 bp)<S7(360 bp)<S1(375 bp)<S4(376 bp)<S3和S5(384 bp)<S8(442 bp)<S9(1323 bp)<S2(1355 bp)。我们分析了S-RNase基因的序列,该基因在相邻外显子之间的高变(HV)区域具有大小各异的内含子,且具有相当高的同源性。内含子大小如下:S1 = 167 bp,S2 = 1153 bp,S3 = 179 bp,S4 = 168 bp,S5 = 179 bp,S6 = 147 bp,S7 = 152 bp,S8 = 234 bp,S9 = 1115 bp。S1、S3、S4、S5、S6和S-RNases的内含子中有五个保守区域和五个高变区域。对这些S-RNases内含子进行两两比较,发现同源性如下:S1-RNase和S4-RNase之间为93.7%,S3-RNase和S5-RNase之间为93.3%,S6-RNase和S7-RNase之间为78.9%。PCR-RFLP和S-RNases测序确定了梨品种的S基因型。新口的S基因型为S4S9,新高的为S3S9,丰水的为S3S5,君水的为S1S5,市原的为S1S8,万岁的为S3S5,新梨的为S3S4,黄金梨的为S3S4,水黄的为S3S5,华山的为S3S5,美黄的为S3S5,城西里的为S5S?,甘露的为S3S5,永川白梨的为S3S4,圆黄的为S3S4,甘川的为S3S5,丹巴的为S3S5,万宝的为S3S4,苏旺白梨的为S3S4,秋黄的为S4S6。梨品种S基因型的信息将用于授粉品种选择和育种计划。