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

Author:

Mönch Tanja C.1,Smylla Thomas K.1ORCID,Brändle Franziska1ORCID,Preiss Anette2ORCID,Nagel Anja C.1ORCID

Affiliation:

1. Department of Molecular Genetics, Institute of Biology, University of Hohenheim, 70599 Stuttgart, Germany

2. Institute of Biology, University of Hohenheim, 70599 Stuttgart, Germany

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.

Funder

Deutsche Forschungsgemeinschaft DFG

University of Hohenheim.

Drosophila Genomics Resource Center DGRC

Developmental Studies Hybridoma Bank

National Human Genome Research Institute and the British Medical Research Council

Publisher

MDPI AG

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