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MEAM2 之困:假基因对全球入侵烟粉虱(半翅目:粉虱科)隐种复合群物种界定的影响。

The Trouble with MEAM2: Implications of Pseudogenes on Species Delimitation in the Globally Invasive Bemisia tabaci (Hemiptera: Aleyrodidae) Cryptic Species Complex.

机构信息

CSIRO, Black Mountain Science and Innovation Park, Acton, Australia.

CIRAD, UMR PVBMT, La Réunion, France.

出版信息

Genome Biol Evol. 2017 Oct 1;9(10):2732-2738. doi: 10.1093/gbe/evx173.

Abstract

Molecular species identification using suboptimal PCR primers can over-estimate species diversity due to coamplification of nuclear mitochondrial (NUMT) DNA/pseudogenes. For the agriculturally important whitefly Bemisia tabaci cryptic pest species complex, species identification depends primarily on characterization of the mitochondrial DNA cytochrome oxidase I (mtDNA COI) gene. The lack of robust PCR primers for the mtDNA COI gene can undermine correct species identification which in turn compromises management strategies. This problem is identified in the B. tabaci Africa/Middle East/Asia Minor clade which comprises the globally invasive Mediterranean (MED) and Middle East Asia Minor I (MEAM1) species, Middle East Asia Minor 2 (MEAM2), and the Indian Ocean (IO) species. Initially identified from the Indian Ocean island of Réunion, MEAM2 has since been reported from Japan, Peru, Turkey and Iraq. We identified MEAM2 individuals from a Peruvian population via Sanger sequencing of the mtDNA COI gene. In attempting to characterize the MEAM2 mitogenome, we instead characterized mitogenomes of MEAM1. We also report on the mitogenomes of MED, AUS, and IO thereby increasing genomic resources for members of this complex. Gene synteny (i.e., same gene composition and orientation) was observed with published B. tabaci cryptic species mitogenomes. Pseudogene fragments matching MEAM2 partial mtDNA COI gene exhibited low frequency single nucleotide polymorphisms that matched low copy number DNA fragments (<3%) of MEAM1 genomes, whereas presence of internal stop codons, loss of expected stop codons and poor primer annealing sites, all suggested MEAM2 as a pseudogene artifact and so not a real species.

摘要

使用非最佳 PCR 引物进行分子物种鉴定可能会因核线粒体 (NUMT) DNA/假基因的共扩增而高估物种多样性。对于农业上重要的粉虱烟粉虱隐种害虫复合体,物种鉴定主要取决于线粒体 DNA 细胞色素氧化酶 I (mtDNA COI) 基因的特征。缺乏用于 mtDNA COI 基因的稳健 PCR 引物会破坏正确的物种鉴定,从而影响管理策略。在包含全球入侵地中海 (MED) 和中东/小亚细亚 1 型 (MEAM1) 种、中东/小亚细亚 2 型 (MEAM2) 和印度洋 (IO) 种的烟粉虱非洲/中东/小亚细亚分支中,就存在这个问题。MEAM2 最初是从印度洋留尼汪岛鉴定出来的,此后在日本、秘鲁、土耳其和伊拉克也有报道。我们通过 mtDNA COI 基因的 Sanger 测序鉴定了秘鲁种群中的 MEAM2 个体。在试图对 MEAM2 线粒体基因组进行特征分析时,我们反而对 MEAM1 的线粒体基因组进行了特征分析。我们还报告了 MED、AUS 和 IO 的线粒体基因组,从而增加了该复合体成员的基因组资源。与已发表的烟粉虱隐种线粒体基因组一样,观察到基因基因座 (即相同的基因组成和方向)。与 MEAM2 部分 mtDNA COI 基因匹配的假基因片段表现出低频率的单核苷酸多态性,与 MEAM1 基因组中低拷贝数 (<3%) 的 DNA 片段匹配,而内部终止密码子的存在、预期终止密码子的丢失和较差的引物退火位点,都表明 MEAM2 是假基因假阳性,而不是真正的物种。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/452f/5647793/85f336c967af/evx173f1.jpg

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