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A male-biased sex-distorter gene drive for the human malaria vector Anopheles gambiae

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TLDR
A male-biased sex-distorter gene drive (SDGD) is reported in the human malaria vector Anopheles gambiae and is predicted to have a quicker impact on female mosquito populations than previously developed gene drives targeting female fertility.
Abstract
Only female insects transmit diseases such as malaria, dengue and Zika; therefore, control methods that bias the sex ratio of insect offspring have long been sought. Genetic elements such as sex-chromosome drives can distort sex ratios to produce unisex populations that eventually collapse, but the underlying molecular mechanisms are unknown. We report a male-biased sex-distorter gene drive (SDGD) in the human malaria vector Anopheles gambiae. We induced super-Mendelian inheritance of the X-chromosome-shredding I-PpoI nuclease by coupling this to a CRISPR-based gene drive inserted into a conserved sequence of the doublesex (dsx) gene. In modeling of invasion dynamics, SDGD was predicted to have a quicker impact on female mosquito populations than previously developed gene drives targeting female fertility. The SDGD at the dsx locus led to a male-only population from a 2.5% starting allelic frequency in 10–14 generations, with population collapse and no selection for resistance. Our results support the use of SDGD for malaria vector control.

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Journal ArticleDOI

Efficient population modification gene-drive rescue system in the malaria mosquito Anopheles stephensi.

TL;DR: A recoded gene-drive rescue system for population modification of the malaria vector, Anopheles stephensi, that relieves the load in females caused by integration of the drive into the kynurenine hydroxylase gene by rescuing its function is developed.
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Modelling the suppression of a malaria vector using a CRISPR-Cas9 gene drive to reduce female fertility

TL;DR: Simulation modelling indicates that considerable suppression of vector populations can be achieved within a few years of using a female sterility gene drive, though the impact is likely to be heterogeneous in space and time.
Journal ArticleDOI

Combating mosquito-borne diseases using genetic control technologies.

TL;DR: A review of the latest developments, notable similarities, and critical distinctions between these promising technologies and discuss their future applications for mosquito-borne disease control can be found in this paper, where the authors discuss the future applications of these technologies.
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Nix alone is sufficient to convert female Aedes aegypti into fertile males and myo-sex is needed for male flight.

TL;DR: The Nix transgene alone, in the absence of the M-locus, was sufficient to convert females into males with all male-specific sexually dimorphic features and male-like gene expression and Nix-mediated female-to-male conversion was 100% penetrant and stable over many generations.
References
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Journal ArticleDOI

NIH Image to ImageJ: 25 years of image analysis

TL;DR: The origins, challenges and solutions of NIH Image and ImageJ software are discussed, and how their history can serve to advise and inform other software projects.
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Extraordinary Sex Ratios

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A CRISPR-Cas9 gene drive system targeting female reproduction in the malaria mosquito vector Anopheles gambiae

TL;DR: Population modeling and cage experiments indicate that a CRISPR-Cas9 construct targeting one of these loci meets the minimum requirement for a gene drive targeting female reproduction in an insect population, which could expedite the development of gene drives to suppress mosquito populations to levels that do not support malaria transmission.
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Highly efficient Cas9-mediated gene drive for population modification of the malaria vector mosquito Anopheles stephensi

TL;DR: A highly effective autonomous Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-associated protein 9 (Cas9)-mediated gene-drive system in the Asian malaria vector Anopheles stephensi, adapted from the mutagenic chain reaction (MCR).
Journal ArticleDOI

Meiotic sex chromosome inactivation

James M. A. Turner
- 15 May 2007 - 
TL;DR: This work has established sex chromosome asynapsis as the primary trigger of MSCI, and it is now clear that it is maintained, although not completely, well beyond meiosis and into sperm development.
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