Bosković Radovan I, Tobutt Kenneth R, Ortega Encarnación, Sutherland Bruce G, Godini Angelo
East Malling Research, New Road, East Malling, Kent ME19 6BJ, UK.
Mol Genet Genomics. 2007 Dec;278(6):665-76. doi: 10.1007/s00438-007-0283-4. Epub 2007 Sep 27.
Prunus dulcis, the almond, is a predominantly self-incompatible (SI) species with a gametophytic self-incompatibility system mediated by S-RNases. The economically important allele Sf, which results in self-compatibility in P. dulcis, is said to have arisen by introgression from Prunus webbii in the Italian region of Apulia. We investigated the range of self-(in)compatibility alleles in Apulian material of the two species. About 23 cultivars of P. dulcis (14 self-compatible (SC) and nine SI) and 33 accessions of P. webbii (16 SC, two SI and 15 initially of unknown status), all from Apulia, were analysed using PCR of genomic DNA to amplify S-RNase alleles and, in most cases, IEF and staining of stylar protein extracts to detect S-RNase activity. Some amplification products were cloned and sequenced. The allele Sf was present in nearly all the SC cultivars of P. dulcis but, surprisingly, was absent from nearly all SC accessions of P. webbii. And of particular interest was the presence in many SI cultivars of P. dulcis of a new active allele, labelled S30, the sequence of which showed it to be the wild-type of Sf so that Sf can be regarded as a stylar part mutant S30 degrees . These findings indicate Sf may have arisen within P. dulcis, by mutation. One SC cultivar of P. dulcis, 'Patalina', had a new self-compatibility allele lacking RNase activity, Sn5, which could be useful in breeding programmes. In the accessions of P. webbii, some of which were known to be SC, three new alleles were found which lacked RNase activity but had normal DNA sequences.
扁桃(Prunus dulcis)是一种主要自交不亲和(SI)的物种,具有由S-核酸酶介导的配子体自交不亲和系统。经济上重要的等位基因Sf导致扁桃自交亲和,据说它是通过从意大利普利亚地区的韦氏李(Prunus webbii)渗入而产生的。我们研究了这两个物种在普利亚材料中的自(不)亲和等位基因范围。对来自普利亚的约23个扁桃品种(14个自交亲和(SC)和9个自交不亲和)以及33个韦氏李种质(16个SC、2个SI和15个初始状态未知)进行了分析,使用基因组DNA的PCR扩增S-核酸酶等位基因,并且在大多数情况下,通过IEF和花柱蛋白提取物染色来检测S-核酸酶活性。一些扩增产物被克隆并测序。等位基因Sf几乎存在于所有扁桃的SC品种中,但令人惊讶的是,几乎不存在于所有韦氏李的SC种质中。特别有趣的是,在许多扁桃的SI品种中存在一个新的活性等位基因,标记为S30,其序列表明它是Sf的野生型,因此Sf可被视为花柱部分突变体S30°。这些发现表明Sf可能是在扁桃内通过突变产生的。扁桃的一个SC品种“Patalina”有一个缺乏核糖核酸酶活性的新自交亲和等位基因Sn5,这在育种计划中可能有用。在韦氏李的种质中,其中一些已知是SC,发现了三个缺乏核糖核酸酶活性但具有正常DNA序列的新等位基因。