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CRISPR disruption of optix in tobacco hawkmoth replaces orange pigmentation with black eumelanin

A preprint extends the known role of the optix transcription factor beyond nymphalid butterflies, showing it controls abdominal melanin patterning in the moth Manduca sexta.

Published · AI-drafted summary based on 1 public source
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Research on colour patterning in Lepidoptera has established a conserved genetic toolkit that includes the homeobox transcription factor optix, previously shown to regulate ommochrome and melanin pigmentation and structural coloration in nymphalid butterflies. Whether optix plays equivalent roles in other insect groups has remained unclear.

A preprint deposited on bioRxiv (20 August 2026) describes the use of CRISPR-Cas9 to disrupt optix in the tobacco hawkmoth Manduca sexta, a species outside the Nymphalidae. Loss of optix function produced a striking abdominal pigmentation phenotype: orange pigmentation was replaced by black eumelanin, confirmed by chemical analysis. The result demonstrates that the role of optix in colour patterning is not confined to nymphalid butterflies and suggests it may act as a broader regulator of lepidopteran pigmentation programmes.

The study contributes to understanding of how a limited set of transcription factors can be repeatedly deployed across distantly related lineages to pattern colour, a question relevant to evolutionary developmental biology and the genetics of adaptation. As a preprint, this work has not yet completed peer review and the findings should be interpreted accordingly.

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  1. Primary sourcePreprint bioRxiv (Cold Spring Harbor Laboratory) · 2026-08-25
    optix regulates abdominal melanin pigmentation in the tobacco hawkmoth Manduca sexta

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pigmentation optix crispr manduca-sexta lepidoptera melanin evo-devo preprint
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Educational summaries of public genetics news

Genetic Current is the news section of Evagene, an academic, research, and educational pedigree-modelling platform. Stories are AI-drafted summaries of items from trusted public sources, written for researchers, clinicians, educators, students, genealogists, and patients with an interest in genetics. Summaries are for educational and research purposes only and are not medical advice.

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