Growth zone segmentation in the milkweed bug Oncopeltus fasciatus sheds light on the evolution of insect segmentation
Auman T, Chipman AD. BMC evolutionary biology, November 2018.
Read the paper Free to read · doi:10.1186/s12862-018-1293-z
What this paper is about
Fruit flies pattern all their body segments at once, which is unusual; most insects add them one at a time. That makes the fly a poor model for how segmentation evolved.
The authors documented the expression of 12 genes through segmentation in the large milkweed bug, which adds segments sequentially.
Summarised here from the abstract below. Not the authors’ words.
Abstract
BackgroundOne of the best studied developmental processes is the Drosophila segmentation cascade. However, this cascade is generally considered to be highly derived and unusual, with segments being patterned simultaneously, rather than the ancestral sequential segmentation mode. We present a detailed analysis of the segmentation cascade of the milkweed bug Oncopletus fasciatus, an insect with a more primitive segmentation mode, as a comparison to Drosophila, with the aim of reconstructing the evolution of insect segmentation modes.ResultsWe document the expression of 12 genes, representing different phases in the segmentation process. Using double staining we reconstruct the spatio-temporal relationships among these genes. We then show knock-down phenotypes of representative genes in order to uncover their roles and position in the cascade.ConclusionsWe conclude that sequential segmentation in the Oncopeltus germband includes three slightly overlapping phases: Primary pair-rule genes generate the first segmental gene expression in the anterior growth zone. This pattern is carried anteriorly by a series of secondary pair-rule genes, expressed in the transition between the growth zone and the segmented germband. Segment polarity genes are expressed in the segmented germband with conserved relationships. Unlike most holometabolous insects, this process generates a single-segment periodicity, and does not have a double-segment pattern at any stage. We suggest that the evolutionary transition to double-segment patterning lies in mutually exclusive expression patterns of secondary pair-rule genes. The fact that many aspects of the putative Oncopeltus segmentation network are similar to those of Drosophila, is consistent with a simple transition between sequential and simultaneous segmentation.
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title = {Growth zone segmentation in the milkweed bug Oncopeltus fasciatus sheds light on the evolution of insect segmentation (listing)},
author = {{Milkweed USA}},
year = {2026},
url = {https://milkweedusa.com/research/growth-zone-segmentation-in-the-milkweed-bug-oncopeltus-fasciatus-2018/},
note = {Accessed DATE}
}