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Regulatory divergences in dosage compensation cause hybrid male inviability in Caenorhabditis

  • Yongbin Li (Co-first author)
  • , Yimeng Gao (Co-first author)
  • , Jiaonv Ma
  • , Yifan Gao
  • , Wangyan Zhou
  • , Hantang Zhang
  • , Wenhua Shao
  • , Zhijin Liu
  • , Zhongying Zhao
  • , Xiao Liu*
  • *Corresponding author for this work

Research output: Working paperPreprint

Abstract

The genetic basis of Haldane’s rule, such as hybrid male incompatibility in XX systems, has long remained elusive. Here, we found that crosses of Caenorhabditis nigoni males with C. briggsae females result in insufficient expression of Cbr-xol-1, an X-linked master switch responsible for sex determination, consequently activating aberrant dosage compensation in males, and ultimately leading to embryonic inviability. Three compensatory divergences result in comparable xol-1 expression levels between the parental species but lethal Cbr-xol-1 underexpression in hybrid male embryos: 1) a less active Cbr-xol-1 promoter than its C. nigoni ortholog; 2) loss of an X-linked xol-1 paralog in C. briggsae; and 3) pseudogenization of a C. briggsae autosomal repressor of xol-1. Our results define an evolutionary scenario of sexual incompatibility leading to hybrid male inviability.

Original languageEnglish
PublisherCold Spring Harbor Laboratory
Number of pages24
DOIs
Publication statusPublished - 8 Feb 2024

Publication series

NamebioRxiv

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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