心材DNA提取及实时荧光定量PCR快速鉴定——以红木(Pterocarpus Indicus)为例

Jihong Zhang, Jiaying Wang, Xu Ying, Xiaoling Lv, Jianhua Wei, Ma Ming, Junxia Cui
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摘要

过去二十年来,非法采伐、砍伐和木材贸易持续增加,导致森林生物多样性下降,一些木材物种灭绝。野龙柏。被列入中华人民共和国国家标准《红木》(GB/T 18107-2017),因其优质的木材被广泛用于生产高档家具、装饰地板和乐器。对于分子物种鉴定,首先要保证木材样本DNA提取的质量和数量。然而,从干燥、老化的木材心材中提取DNA是困难的,因为心材含有很少的DNA碎片,以及许多已知会阻碍序列扩增的酚类化合物。为了防止籼稻被过度开发,实现准确的种级鉴定,本研究建立了一种从心材样品中提取可扩增DNA的特殊提取方法,并建立了籼稻种级鉴别的实时PCR检测方法。改进的CTAB法提取干心材样品DNA的数量和质量分别为2.40 ~ 37.70 ng/µL和1.55 ~ 2.12 ng/µL (OD值为260/280)。引物组P9在新建立的实时PCR中可扩增,该引物组针对籼稻特有的微卫星Pin2-20序列。分析结果表明,该实时PCR具有特异性和敏感性,检测限约为0.17 ng/µL。希望本研究能够为心材DNA提取和物种鉴定提供依据,为法医鉴定、执法和自然资源保护提供依据。
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DNA Extraction from Heartwood and Quick Species Authentication Using Real-Time PCR: A Case Study of the Rosewood (Pterocarpus Indicus)
: Illegal logging, felling and timber trade have continued to increase over the past two decades, leading to a decline in forest biodiversity and the extinction of some wood species. Pterocarpus indicus Willd., listed in the National Standards of the People’s Republic of China for Hongmu (GB/T 18107-2017), is widely used in production of high-end furniture, decorative flooring and musical instruments due to its high-quality timber. For molecular species identification, the quality and quantity of DNA extracted from wood samples should first be ensured. However, extracting DNA from dried, aged timber heartwood is difficult, as heartwood contains little fragmented DNA, along with lots of phenolic compounds known to impede sequence amplification. In order to protect P. indicus from over-exploitation and to achieve accurate species-level identification, we established a particular extraction method for obtaining amplifiable DNA from heartwood samples and the real-time PCR assay for species discrimination of P. indicus in this study. The quantity and quality of DNA extracted from dry heartwood samples using the modified CTAB method were 2.40-37.70 ng/µL and 1.55-2.12 demonstrated by OD 260/280 , respectively. Primer set P9, targeting P. indicus specific microsatellite Pin2-20 sequence, was amplifiable in newly established real-time PCR. Through analysis, this real time PCR was shown to be specific and sensitive with a detection limit around 0.17 ng/µL. Hopefully, this study will contribute to heartwood DNA extraction and species identification of timber logs for forensic discrimination, law enforcement and natural resource conservation.
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