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标记辅助作图可用于埃及伊蚊正向遗传学分析,该蚊是一种具有广泛重组荒漠的虫媒病毒载体。

Marker-assisted mapping enables forward genetic analysis in Aedes aegypti, an arboviral vector with vast recombination deserts.

机构信息

Genetics Bioinformatics and Computational Biology Program, Virginia Tech, Blacksburg, VA 24061, USA.

Fralin Life Sciences Institute, Virginia Tech, Blacksburg, VA 24061, USA.

出版信息

Genetics. 2022 Nov 1;222(3). doi: 10.1093/genetics/iyac140.

Abstract

Aedes aegypti is a major vector of arboviruses that cause dengue, chikungunya, yellow fever, and Zika. Although recent success in reverse genetics has facilitated rapid progress in basic and applied research, integration of forward genetics with modern technologies remains challenging in this important species, as up to 47% of its chromosome is refractory to genetic mapping due to extremely low rate of recombination. Here, we report the development of a marker-assisted mapping strategy to readily screen for and genotype only the rare but informative recombinants, drastically increasing both the resolution and signal-to-noise ratio. Using marker-assisted mapping, we mapped a transgene that was inserted in a >100-Mb recombination desert and a sex-linked spontaneous red-eye (re) mutation just outside the region. We subsequently determined, by CRISPR/Cas9-mediated knockout, that cardinal is the causal gene of re, which is the first forward genetic identification of a causal gene in Ae. aegypti. The identification of the causal gene of the sex-linked re mutation provides the molecular foundation for using gene editing to develop versatile and stable genetic sexing methods. To facilitate genome-wide forward genetics in Ae. aegypti, we generated and compiled a number of lines with markers throughout the genome. Thus, by overcoming the challenges presented by the vast recombination deserts and the scarcity of markers, we have shown that effective forward genetic analysis is increasingly feasible in this important arboviral vector species.

摘要

埃及伊蚊是一种主要的虫媒病毒载体,可引起登革热、基孔肯雅热、黄热病和寨卡病毒。尽管最近在反向遗传学方面取得了成功,促进了基础和应用研究的快速进展,但正向遗传学与现代技术的整合在这个重要物种中仍然具有挑战性,因为高达 47%的染色体由于极低的重组率而无法进行遗传作图。在这里,我们报告了一种标记辅助作图策略的发展,该策略可以方便地筛选和基因型仅罕见但信息丰富的重组体,极大地提高了分辨率和信噪比。使用标记辅助作图,我们对插入在> 100 Mb 重组沙漠中的转基因和性连锁自发红眼(re)突变进行了作图,该突变刚好位于该区域之外。随后,我们通过 CRISPR/Cas9 介导的敲除确定,cardinal 是 re 的致病基因,这是 Ae. aegypti 中第一个正向遗传鉴定的致病基因。性连锁 re 突变的致病基因的确定为利用基因编辑开发多功能和稳定的遗传性别鉴定方法提供了分子基础。为了促进 Ae. aegypti 中的全基因组正向遗传学,我们生成并编译了许多具有基因组标记的系。因此,通过克服巨大的重组沙漠和标记稀缺带来的挑战,我们表明在这个重要的虫媒病毒载体物种中,有效的正向遗传分析越来越可行。

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