Compton Austin, Sharma Atashi, Hempel Melanie, Aryan Azadeh, Biedler James K, Potters Mark B, Chandrasegaran Karthikeyan, Vinauger Clément, Tu Zhijian
Department of Biochemistry, Virginia Tech, Blacksburg, VA 24061.
The Fralin Life Sciences Institute, Virginia Tech, Blacksburg, VA 24061.
Proc Natl Acad Sci U S A. 2025 May 13;122(19):e2412149122. doi: 10.1073/pnas.2412149122. Epub 2025 May 8.
Diverse genetic strategies are being pursued to control mosquito-borne infectious diseases. These strategies often rely on the release of nonbiting males to either reduce the target mosquito population or render them resistant to pathogens. Male-only releases are important as any contaminating females can bite and potentially transmit pathogens. Despite significant efforts, it remains a major bottleneck to reliably and efficiently separate males from females, especially when nontransgenic males are preferred. In the yellow fever mosquito , sex is determined by a pair of homomorphic sex chromosomes, with the dominant male-determining locus (the M locus) and its counterpart (the m locus) embedded in an M-bearing and an m-bearing chromosome 1, respectively. We utilized both naturally occurring and engineered sex-linked recessive lethal alleles (RLAs) to create sex separation strains for on the basis of differential elimination of marked sex chromosomes (DeMark). DeMark strains are self-sustaining and produce nontransgenic males that are readily separated from individuals carrying RLA- and transgene-marked m chromosomes. For example, the marked m chromosome in the heterozygous mother in some strains was only inherited by her female progeny due to RLA-mediated incompatibility with the M-bearing chromosome in the father, producing nontransgenic males and transgenic females, generation after generation. We further explore strategies to conditionally eliminate females that contain marked sex chromosomes. We also discuss DeMark designs that are applicable for efficient sex separation in organisms with well-differentiated X and Y chromosomes, such as the mosquitoes.
人们正在探索多种基因策略来控制蚊媒传染病。这些策略通常依赖于释放不叮咬的雄性蚊子,以减少目标蚊子种群数量或使其对病原体产生抗性。只释放雄性蚊子很重要,因为任何混杂其中的雌性蚊子都可能叮咬并传播病原体。尽管付出了巨大努力,但可靠且高效地将雄性与雌性蚊子分离仍然是一个主要瓶颈,尤其是在更倾向于使用非转基因雄性蚊子的情况下。在埃及伊蚊中,性别由一对同态性染色体决定,显性雄性决定位点(M位点)及其对应位点(m位点)分别位于携带M和m的1号染色体上。我们利用天然存在的和工程改造的性连锁隐性致死等位基因(RLA),基于标记性染色体的差异消除(DeMark)创建了性别分离品系。DeMark品系能够自我维持,并产生易于与携带RLA和转基因标记m染色体的个体分离的非转基因雄性蚊子。例如,在某些品系中,杂合母体中的标记m染色体仅由其雌性后代遗传,这是由于RLA介导的与父本携带M染色体的不相容性,从而一代又一代地产生非转基因雄性蚊子和转基因雌性蚊子。我们进一步探索有条件地消除含有标记性染色体的雌性蚊子的策略。我们还讨论了适用于在具有高度分化的X和Y染色体的生物体(如按蚊)中进行高效性别分离的DeMark设计。