The neuroblast timer gene nubbin exhibits functional redundancy with gap genes to regulate segment identity in Tribolium

Development. 2021 Aug 15;148(16):dev199719. doi: 10.1242/dev.199719. Epub 2021 Aug 20.

Abstract

The neuroblast timer genes hunchback, Krüppel, nubbin and castor are expressed in temporal sequence in neural stem cells, and in corresponding spatial sequence along the Drosophila blastoderm. As canonical gap genes, hunchback and Krüppel play a crucial role in insect segmentation, but the roles of nubbin and castor in this process remain ambiguous. We have investigated the expression and functions of nubbin and castor during segmentation in the beetle Tribolium. We show that Tc-hunchback, Tc-Krüppel, Tc-nubbin and Tc-castor are expressed sequentially in the segment addition zone, and that Tc-nubbin regulates segment identity redundantly with two previously described gap/gap-like genes, Tc-giant and Tc-knirps. Simultaneous knockdown of Tc-nubbin, Tc-giant and Tc-knirps results in the formation of ectopic legs on abdominal segments. This homeotic transformation is caused by loss of abdominal Hox gene expression, likely due to expanded Tc-Krüppel expression. Our findings support the theory that the neuroblast timer series was co-opted for use in insect segment patterning, and contribute to our growing understanding of the evolution and function of the gap gene network outside of Drosophila.

Keywords: Tribolium castaneum; castor; nubbin; Gap gene; Hox gene; Neuroblast.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blastoderm / metabolism
  • Body Patterning / genetics*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Drosophila / genetics
  • Drosophila / growth & development
  • Embryonic Development / genetics
  • Female
  • Gene Expression
  • Gene Expression Regulation, Developmental
  • Gene Regulatory Networks
  • Genes, Homeobox*
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / metabolism
  • Insect Proteins / genetics*
  • Insect Proteins / metabolism
  • Male
  • Neural Stem Cells / metabolism*
  • POU Domain Factors / genetics*
  • POU Domain Factors / metabolism
  • RNA Interference
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Tribolium / embryology*
  • Tribolium / genetics*

Substances

  • DNA-Binding Proteins
  • Homeodomain Proteins
  • Insect Proteins
  • POU Domain Factors
  • Repressor Proteins

Associated data

  • figshare/10.6084/m9.figshare.14762025
  • figshare/10.6084/m9.figshare.14770179