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Biology subjects

Carvalho, C. A.

Publications and source records attributed to Carvalho, C. A..

2 recordsLinked to original sources

Adherens junctions limit the extent of the septate junctions in Drosophila midgut enterocytes but are not required for apical-basal polarity

Adherens junctions formed by E-cadherin adhesion complexes play central roles in the organisation and apical-basal polarisation of both mammalian and insect epithelia. Here we investigate the function of the components of the E-cadherin adhesion complex in the Drosophila midgut epithelium, which establishes polarity by a different mechanism from other fly epithelia and has an inverted junctional arrangement, in which the adherens junctions lie below the septate junctions. Unlike other epithelial tissues, loss of E-cadherin, Armadillo ({beta}-catenin) or -catenin has no effect on the polarity or organisation of the adult midgut epithelium. This is not due to redundancy with N-cadherin, providing further evidence that the midgut polarises in distinct way from other epithelia. However, E-cadherin (shg) and armadillo mutants have an expanded septate junction domain and a smaller lateral domain below the septate junctions. Thus, E-cadherin adhesion complexes limit the basal extent of the septate junctions. This function does not appear to depend on the linkage of E-cadherin to the actin cytoskeleton because -catenin mutants do not significantly perturb the relative sizes of the septate and sub-septate junction domains.

cell biology↗

SUMO-mediated regulation of a H3K4me3 reader controls germline development in C. elegans

ULP-2 is a conserved SUMO protease required for embryonic development in C. elegans. Here we revealed that ULP-2 controls germline development by regulating the PHD-SET domain protein, SET-26. Specifically, the ulp-2 mutant hermaphrodites exhibit increased sterility and progressive elevation in global protein sumoylation. In the progeny of homozygous animals, meiosis is arrested at the diplotene stage and the cells in the proximal germline acquire a somatic fate. Germline RNAseq analysis revealed the downregulation of numerous germline genes, whereas somatic gene expression is upregulated in ulp-2 mutant gonads. To determine the key factors that are regulated by ULP-2, we performed a yeast two-hybrid screen and identified the H3K4me3 reader, SET-26. Genetic interaction was observed in double mutant ulp-2;set-26 resulting in enhanced sterility phenotype to complete sterility in the first generation of homozygous offspring. Consistently, SET-26 is sumoylated and its sumoylation levels are regulated by ULP-2. Moreover, we detected reduction in H3K4me3 levels bound to SET-26 in the ulp-2 mutant background. A comparative proteomics screen between WT and ulp-2 loss of activity identified the predicted methyltransferase SET-27 as a ULP-2-dependent SET-26-associated protein. SET-27 knockout genetically interacts with ULP-2 in the germline, but not with SET-26. Taken together, we revealed a ULP-2/SET-26 axis which is required for the maintenance and regulation of germline development.

cell biology↗