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利用细胞色素 b 基因的短序列区分现存大象象牙和猛犸象牙。

Distinguishing extant elephants ivory from mammoth ivory using a short sequence of cytochrome b gene.

机构信息

College of Wildlife and Protected Areas, Northeast Forestry University, Harbin, 150040, China.

BGI - Shenzhen, Shenzhen, 518083, China.

出版信息

Sci Rep. 2019 Dec 11;9(1):18863. doi: 10.1038/s41598-019-55094-x.

Abstract

Trade in ivory from extant elephant species namely Asian elephant (Elephas maximus), African savanna elephant (Loxodonta africana) and African forest elephant (Loxodonta cyclotis) is regulated internationally, while the trade in ivory from extinct species of Elephantidae, including woolly mammoth, is unregulated. This distinction creates opportunity for laundering and trading elephant ivory as mammoth ivory. The existing morphological and molecular genetics methods do not reliably distinguish the source of ivory items that lack clear identification characteristics or for which the quality of extracted DNA cannot support amplification of large gene fragments. We present a PCR-sequencing method based on 116 bp target sequence of the cytochrome b gene to specifically amplify elephantid DNA while simultaneously excluding non-elephantid species and ivory substitutes, and while avoiding contamination by human DNA. The partial Cytochrome b gene sequence enabled accurate association of ivory samples with their species of origin for all three extant elephants and from mammoth. The detection limit of the PCR system was as low as 10 copy numbers of target DNA. The amplification and sequencing success reached 96.7% for woolly mammoth ivory and 100% for African savanna elephant and African forest elephant ivory. This is the first validated method for distinguishing elephant from mammoth ivory and it provides forensic support for investigation of ivory laundering cases.

摘要

贸易象牙从现存的大象物种,即亚洲象(Elephas maximus)、非洲草原象(Loxodonta africana)和非洲森林象(Loxodonta cyclotis),受到国际管制,而从已灭绝的象科物种,包括猛犸象,贸易象牙不受管制。这种区别为将象牙作为猛犸象牙进行洗钱和交易创造了机会。现有的形态学和分子遗传学方法不能可靠地区分缺乏明确鉴定特征的象牙制品的来源,或者提取的 DNA 质量不能支持扩增大片段基因的来源。我们提出了一种基于细胞色素 b 基因 116bp 靶序列的 PCR-测序方法,该方法可以特异性地扩增象科 DNA,同时排除非象科物种和象牙替代品,并且避免人类 DNA 的污染。部分细胞色素 b 基因序列使象牙样本能够准确地与其来源物种相关联,包括三种现存的大象和猛犸象。该 PCR 系统的检测限低至目标 DNA 的 10 个拷贝数。扩增和测序成功率达到 96.7%的猛犸象象牙和 100%的非洲草原象和非洲森林象象牙。这是第一种用于区分象牙和猛犸象牙的验证方法,为象牙洗钱案件的调查提供了法医支持。

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