首页> 外文期刊>Annals of Applied Biology >Detection of Coconut cadang-cadang viroid sequences in oil and coconut palm by ribonuclease protection assay.
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Detection of Coconut cadang-cadang viroid sequences in oil and coconut palm by ribonuclease protection assay.

机译:核糖核酸酶保护法检测椰子和椰子油中椰子豆类-椰子类病毒的序列。

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A ribonuclease protection assay (RPA) has been developed for detecting Coconut cadang-cadang viroid (CCCVd) sequences. An RNA probe complementary to full-length CCCVd246 was used, terminating at nucleotide 65 in the upper conserved region, and linked to a non-viroid 5' sequence, which acted as an internal control for ribonuclease activity. Extracts from CCCVd-infected coconut (Cocos nucifera) and African oil (Elaeis guineensis) palms protected three major fragments of approximately 250, 125 and 50 nt and a variable number of minor fragments. Extracts of healthy coconut palms, Potato spindle tuber viroid-infected tomato and transfer RNA did not protect the probe. The approximately 250 nt fragment is predicted to indicate the presence of monomers and dimers of circular CCCVd246, linear CCCVd246 with the same termini as the probe and point mutants of these forms. The origin of smaller protected fragments is discussed. RPA-detected CCCVd sequences in 13 of 18 oil palms surveyed in a commercial plantation in Malaysia. Signal intensity varied between the positive oil palms and was generally lower than in coconut palms infected with CCCVd. An infection phenotype was implied but not confirmed by the observation that in a group of 10 oil palms with orange leaf spotting, 9 contained CCCVd, whereas in a group of 8 palms without orange spotting, the viroid was detected in 4. Of four coconut palms in Sri Lanka shown by dot-blot assay to contain CCCVd-related RNA, one was shown by RPA to be positive for the CCCVd246 sequence. RPA is therefore a robust and sensitive test for CCCVd sequences, and our results show that sequences closely related to CCCVd246 are not confined to the Philippines.
机译:已经开发了一种核糖核酸酶保护测定法(RPA),用于检测椰子cadang-cadang病毒(CCCVd)序列。使用了与全长CCCVd 246 互补的RNA探针,该探针终止于上保守区的核苷酸65处,并与非病毒5'序列连接,该序列充当核糖核酸酶活性的内部对照。受CCCVd感染的椰子( Cocos nucifera )和非洲油( Elaeis guineensis )棕榈的提取物保护了大约250、125和50 nt的三个主要片段以及数量不等的次要片段碎片。健康的椰子树,马铃薯纺锤形块茎类病毒感染的番茄和转移RNA的提取物不能保护探针。预测约250 nt的片段指示存在环状CCCVd 246 ,线性CCCVd 246 的单体和二聚体,其末端与这些形式的探针和点突变体相同。讨论了较小的受保护片段的起源。在马来西亚一家商业种植园中,对18种油棕中的13种进行RPA检测的CCCVd序列。阳性油棕之间的信号强度各不相同,通常低于感染CCCVd的椰子棕。暗示了感染表型,但没有观察到感染表型,在观察到的10个油棕中发现橙色斑点的油棕中,有9个含有CCCVd,而在8个油棕中没有发现橙色斑点的油棕中,在4个椰子中发现了类病毒。通过斑点印迹法在斯里兰卡发现含有CCCVd相关的RNA,RPA显示其中一个对CCCVd 246 序列呈阳性。因此,RPA是对CCCVd序列的可靠且灵敏的测试,我们的结果表明,与CCCVd 246 紧密相关的序列不限于菲律宾。

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