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Monitoring adventitious presence of transgenes in brinjal (Solanum melongena L.) collections from the regions in India bordering Bangladesh: a case report

机译:监测来自印度地区的Brinjal(Solanum Melongena L.)收藏的Transgenes的太定存在性接触孟加拉国的地区:案例报告

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India has been predicted as a center of origin of brinjal (Solanum melongena L.) with large number of wild and weedy relatives distributed across the Indian subcontinent. Fruit and Shoot Borer (FSB) is one of the most devastating insect pests of brinjal causing production losses up to 80%. Bt technology has played a key role in imparting FSB resistance in brinjal. In 2013, Bt brinjal event EE1 was commercialized in Bangladesh. Since the neighbouring country shares porous borders with north-eastern states of India, it is important to check for any unapproved entry of genetically modified (GM) brinjal in India. Adventitious presence of transgenes was monitored in the samples collected from regions of Assam, Meghalaya, Mizoram, Tripura and West Bengal bordering Bangladesh. A total of 211 brinjal samples were collected from 32 locations of selected states. Conventional singleplex and multiplex PCR assays and real time PCR were employed to target the genetic elements of Bt Brinjal viz. cry1Ac transgene, Cauliflower Mosaic Virus 35S promoter (P-35S), neomycin phosphotransferase II (nptII) and aminoglycoside-3 '-adenyltransferase (aadA) marker genes. Based on the tests conducted, adventitious presence of transgenes was not detected in any of the collected samples. This approach targeting common screening elements or specific GM target could be efficiently employed to check for unapproved GM events in food and supply chain to comply with the regulatory requirements.
机译:印度被预测为Brinjal(Solanum Melongena L.)的起源中心,其中大量野生和杂草亲属分布在印度次大陆。水果和射击钻孔(FSB)是Brinjal最毁灭性的害虫害虫之一,导致生产损失高达80%。 BT技术在赋予布林格省的FSB电阻方面发挥了关键作用。 2013年,BT Brinjal活动EE1在孟加拉国商业化。由于邻近国家与印度东北国与印度东部的多孔边界共享,因此在印度检查任何未经批准的遗传修改(GM)Brinjal的进入。在从阿萨姆,Meghalaya,Mizoram,Tripura和West Bengal接近孟加拉国的地区收集的样本中监测转基因的太定存在。从32个选定状态的32个位置收集了总共211个Brinjal样品。使用常规的单络和多重PCR测定和实时PCR靶向BT Brinjal Ziz的遗传元素。 Cry1AC转基因,花椰菜马赛克病毒35s启动子(P-35s),新霉素磷酸转移酶II(NPTII)和氨基糖苷-3' - 腺苷转移酶(AADA)标记基因。基于进行的测试,在任何收集的样品中未检测到转基因的不定程存在。可以有效地使用该方法,以统计公共筛查元素或特定的GM目标,以检查食品和供应链中的未批准的通用机组事件,以符合监管要求。

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