# Novel Genome-Engineered H Alleles Differentially Affect Lateral Inhibition and Cell Dichotomy Processes during Bristle Organ Development

**Authors:** Tanja C. Mönch, Thomas K. Smylla, Franziska Brändle, Anette Preiss, Anja C. Nagel

PMC · DOI: 10.3390/genes15050552 · 2024-04-26

## TL;DR

This paper studies how different mutations in the Hairless gene affect bristle development in fruit flies.

## Contribution

The study introduces new Hairless alleles and reveals distinct roles in lateral inhibition and cell specification.

## Key findings

- HWA affects only lateral inhibition, while HNN also impacts cell type specification.
- Reduced Su(H) dosage suppresses HNN but amplifies HWA bristle defects.
- HWA and HNN mutants show distinct bristle organ transformations.

## Abstract

Hairless (H) encodes the major antagonist in the Notch signaling pathway, which governs cellular differentiation of various tissues in Drosophila. By binding to the Notch signal transducer Suppressor of Hairless (Su(H)), H assembles repressor complexes onto Notch target genes. Using genome engineering, three new H alleles, HFA, HLLAA and HWA were generated and a phenotypic series was established by several parameters, reflecting the residual H-Su(H) binding capacity. Occasionally, homozygous HWA flies develop to adulthood. They were compared with the likewise semi-viable HNN allele affecting H-Su(H) nuclear entry. The H homozygotes were short-lived, sterile and flightless, yet showed largely normal expression of several mitochondrial genes. Typical for H mutants, both HWA and HNN homozygous alleles displayed strong defects in wing venation and mechano-sensory bristle development. Strikingly, however, HWA displayed only a loss of bristles, whereas bristle organs of HNN flies showed a complete shaft-to-socket transformation. Apparently, the impact of HWA is restricted to lateral inhibition, whereas that of HNN also affects the respective cell type specification. Notably, reduction in Su(H) gene dosage only suppressed the HNN bristle phenotype, but amplified that of HWA. We interpret these differences as to the role of H regarding Su(H) stability and availability.

## Linked entities

- **Genes:** LOC101253443 (protein SRA1) [NCBI Gene 101253443], FUT1 (fucosyltransferase 1 (H blood group)) [NCBI Gene 2523], RBPJ (recombination signal binding protein for immunoglobulin kappa J region) [NCBI Gene 3516], Notch (neurogenic locus notch homolog) [NCBI Gene 100616083]
- **Species:** Drosophila (taxon 7215)

## Full-text entities

- **Genes:** N (Notch) [NCBI Gene 31293] {aka 1.1, 16-178, 16-55, Ax, CG3936, CT13012}, Su(H) (Suppressor of Hairless) [NCBI Gene 34881] {aka BG:DS00929.10, C, CBF1, CG3497, CSL, D}
- **Species:** Drosophila melanogaster (fruit fly, species) [taxon 7227]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11121709/full.md

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Source: https://tomesphere.com/paper/PMC11121709