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Table 1 The details of RNAi accessory genes duplicated in the obscura group as reported by Palmer et al. [23]

From: Widespread gene duplication and adaptive evolution in the RNA interference pathways of the Drosophila obscura group

Gene

Involvement in piRNA pathway

Function of the protein product

Tissue expression in Dmel

Reference

armitage (armi)

piRNA biogenesis

A RNA helicase which unwinds the piRNA intermediates before loading into Piwi

ubiquitously expressed, highest in ovary

[30]

[31]

asterix (arx)

TGS (Transcriptional Gene Silencing)

A zinc-finger protein which directly interacts with Piwi to scan and identify the transposon transcriptions as target for histone modifications

ubiquitously expressed, highest in ovary

[32]

[33]

cutoff (cuff)

piRNA transcription

Forms a complex with Rhino-Deadlock-Cutoff (Rhi-Del-Cuff) to protect uncapped non-canonical (dual-strand cluster) piRNA transcript from degradation, splicing and transcription termination

testis

[34]

maelstrom (mael)

TGS

Act downstream of Piwi to establish histone modification and prevent the spreading of the silencing marker to the surrounding genes

brain, testis, adult female salivary gland, ovary

[35]

tejas (tej)

Secondary piRNA production (Ping-pong cycle)

A Tudor-domain protein which physically interact with Vas, Spn-E and Aub for a proper ping-pong cycle in the nuage

testis, accessory glands, adult female salivary gland, ovary

[36]

vreteno (vret)

piRNA biogenesis

A Tudor-domain protein which essential for an early primary piRNA processing

larval brain, adult female salivary gland, ovary, testis

[37]

  1. The tissue gene expression in Dmel is based on the FlyAtlas2 [38]. We report tissues with enrichment > 0.4