深色基因编辑触发了Ceratitis capitata中对温度敏感的致命表型.
Germano Sollazzo1,2,3, Katerina Nikolouli1, Georgia Gouvi1,4,3
1Insect Pest Control Laboratory, Joint FAO/IAEA Centre of Nuclear Techniques in Food and Agriculture, Friedensstrasse 1, Seibersdorf, 2444, Austria.
BMC biotechnology
|February 2, 2024
概括
研究人员确定了地中海果中的深色基因是开发温度敏感致命 (tsl) 特性的候选者. 基因编辑成功地创造了TSL突变菌株,为在害虫控制中创建基因性别定性菌株 (GSS) 提供了一个新的工具.
科学领域:
- 昆虫学 昆虫学是一门学科.
- 遗传学 遗传学 是一个
- 虫害管理 虫害管理 虫害管理
背景情况:
- 地中海果 (Ceratitis capitata) 是一个主要的农业害虫.
- 全面综合害虫管理 (AW-IPM) 和无菌昆虫技术 (SIT) 是关键的控制策略.
- 基因性别定性菌株 (GSS) 通过允许仅限男性的释放来提高SIT效率.
研究的目的:
- 为了研究深色 (Ccdor) 基因作为温度敏感致命 (tsl) 现型的候选者.
- 开发一种使用可选择标记器构建GSS的通用方法.
- 为了识别和描述 GSS 开发中的 Ccdor 中的突变.
主要方法:
- 细胞遗传学,基因组学和生物信息学被用来定位和描述Ccdor基因.
- 使用CRISPR/Cas9基因编辑 (NHEJ和HDR) 来诱导Ccdor.中的突变.
- 突变菌株在不同温度下对TSL表型和健康成本进行了评估.
主要成果:
- 该Ccdor基因定位在假定TSL区域的5号染色体上.
- 在CRISPR/Cas9基因编辑中,Ccdor突变菌株表现出TSL表型.
- 开发的菌株在标准养殖温度 (25°C) 时表现出最小的健康成本,在高温 (36°C) 时表现出完全的致命性.
结论:
- 深色基因的基因编辑成功地产生了状炎中温度敏感的致命突变菌株.
- 这些发现表明,保存的深色基因是开发新型GSS的可行目标.
- 这种方法有可能在其他昆虫害虫和疾病载体中产生GSS.
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