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无辣品种(系)中的辣椒素合成酶的基因缺失有利于用SCAR标记早期检测辣度
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作者 Choong-Jae lee Eun Young Yoo +1 位作者 Joo Hyun Shin 泛舟 《辣椒杂志》 2005年第4期45-48,共4页
用辣椒品种ECW123R(C.annuum)与CM334(C.annuum)杂交,对其121个F2代单株进行的检测表明,辣椒素合成酶基因(CS)与C位点的共分离控制了辣味的表达。故我们认为CS与C紧密连锁。对四个辣味型品种和四个无辣味型品种的测序分析表明,无辣味型... 用辣椒品种ECW123R(C.annuum)与CM334(C.annuum)杂交,对其121个F2代单株进行的检测表明,辣椒素合成酶基因(CS)与C位点的共分离控制了辣味的表达。故我们认为CS与C紧密连锁。对四个辣味型品种和四个无辣味型品种的测序分析表明,无辣味型品种在CS的5’上游区有一长度为2529bp的缺失(基因序列)存在。我们已研究出该C位点的分子标记,可在植株苗期检测其辣度。根据该缺失序列,我们开发了5个SCAR标志,其中有两个为共显性。这些SCAR标记对早期检测无辣味型个体既方便又准确。 展开更多
关键词 辣椒素合成酶(CS) 辣椒(C.annuum) 辣昧(辣度) 序列特征扩增区标记(SCAR)
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条形柄锈菌34号生理小种的分子标记 被引量:1
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作者 宋晓盼 包喜悦 +1 位作者 刘玉洋 胡小平 《菌物学报》 CAS CSCD 北大核心 2022年第10期1672-1679,共8页
条形柄锈菌Puccinia striiformis f.sp.tritici 34号生理小种(CYR34)是目前我国毒性谱最宽、毒性最强的生理小种,对小麦生产和抗病品种选育造成了极大的影响。本研究采用RAPD-SCAR分子标记技术,从300条RAPD随机引物中筛选到CYR34的特异... 条形柄锈菌Puccinia striiformis f.sp.tritici 34号生理小种(CYR34)是目前我国毒性谱最宽、毒性最强的生理小种,对小麦生产和抗病品种选育造成了极大的影响。本研究采用RAPD-SCAR分子标记技术,从300条RAPD随机引物中筛选到CYR34的特异引物,通过特异性片段回收、克隆和测序(GenBank登录号为OL907303),依据序列设计出了S2008F34/S2008R34特异性引物,能够从CYR34及接种CYR34的小麦发病叶片总DNA中都扩增出417bp的目标片段。采用该特异性引物检测2021年陕西渭南、咸阳和宝鸡地区小麦条锈菌CYR34的流行频率分别为8.6%、6.0%和10.8%。该项研究为小麦条锈菌CYR34号生理小种的快速检测提供了技术支撑。 展开更多
关键词 小麦条锈病 随机多态性DNA 序列特征扩增区 流行频率 分子检测
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Designing a SCAR molecular marker for monitoring Trichoderma cf. harzianum in experimental communities
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作者 Gabriel PéREZ Valentina VERDEJO +2 位作者 Clarissa GONDIM-PORTO Julieta ORLANDO Margarita CARú 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2014年第11期966-978,共13页
Several species of the fungal genus Trichoderma establish biological interactions with various micro- and macro-organisms. Some of these interactions are relevant in ecological terms and in biotechnological applicatio... Several species of the fungal genus Trichoderma establish biological interactions with various micro- and macro-organisms. Some of these interactions are relevant in ecological terms and in biotechnological applications, such as biocontrol, where Trichoderma could be considered as an invasive species that colonizes a recipient community. The success of this invasion depends on multiple factors, which can be assayed using experimental communities as study models. Therefore, the aim of this work is to develop a species-specific sequence-characterized amplified region (SCAR) marker to monitor the colonization and growth of T. cf. harzianum when it invades experi- mental communities. For this study, 16 randomly amplified polymorphic DNA (RAPD) primers of 10-mer were used to generate polymorphic patterns, one of which generated a band present only in strains of T. cf. harzianum. This band was cloned, sequenced, and five primers of 20-23 mer were designed. Primer pairs 2F2/2R2 and 2F2/2R3 successfully and specifically amplified fragments of 278 and 448 bp from the T. cf. harzianum BpT10a strain DNA, respectively. Both primer pairs were also tested against the DNA from 14 strains of T. cf. harzianum and several strains of different fungal genera as specificity controls. Only the DNA from the strains of T. cf. hat-zianum was successfully amplified. Moreover, primer pair 2F2/2R2 was assessed by quantitative real-time polymerase chain reaction (PCR) using fungal DNA mixtures and DNA extracted from fungal experimental communities as templates. T. cf. harzianum was detectable even when as few as 100 copies of the SCAR marker were available or even when its population represented only 0.1% of the whole community. 展开更多
关键词 Tnchoderma cf. harzianum Sequence-characterized amplified region (SCAR) Molecular marker Experimental fungal communities
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