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Roganowicz, K.

Publications and source records attributed to Roganowicz, K..

2 recordsLinked to original sources

The Ca2+-binding protein CSE links Ca2+-signaling with cell-cell communication in multicellular cyanobacteria

Abstract/SummaryBecause of their multicellular lifestyle, filamentous cyanobacteria have evolved sophisticated cell-cell communication machinery to exchange, synchronize, and coordinate the efforts of individual cells in the filament. Analogous to gap junctions that were regarded as a purely Eukaryotic feature, multicellular cyanobacteria were found also to coordinate their cell-cell communication via septal junctions (SJs). However, the molecular signals that regulate the cell-cell communication machinery and SJs assembly are largely unknown. Lately, Ca2+- signaling has been implicated in regulating cell junctions in neurons. We recently discovered a new Ca2+-sensor protein, CSE, exclusively found in multicellular cyanobacteria. Here, we investigated CSE as a potential link between intracellular Ca2+-signaling and cell-cell communication. We solved the solution NMR structure of CSE in its Ca2+-bound state and revealed that CSE acts as Ca2+-buffer protein. Using cryo-electron tomography, we showed that CSE is not only essential for Ca2+ homeostasis, but also mediates cell-cell communication via regulating the formation of nanopores -- a necessary precursor of SJs -- as {Delta}cse mutant shows a strong reduction in the number of both nanopores and SJs. This determines for the first time Ca2+-signaling as a novel mechanism controlling cell-cell communication and establishes CSE as a key player regulating cyanobacterial multicellularity. This highlights also Ca2+-signaling as a common conserved principle for regulating cell junctions between organisms that deviated billion years ago.

microbiology↗

Structural Insights into the Roles of PARP4 and NAD+ in the Human Vault Cage

Vault is a massive ribonucleoprotein complex found across Eukaryota. The major vault protein (MVP) oligomerizes into an ovular cage, which contains several minor vault components (MVCs) and is thought to transport transiently bound "cargo" molecules. Vertebrate vaults house a poly (ADP-ribose) polymerase (known as PARP4 in humans), which is the only MVC with known enzymatic activity. Despite being discovered decades ago, the molecular basis for PARP4s interaction with MVP remains unclear. In this study, we determined the structure of the human vault cage in complex with PARP4 and its enzymatic substrate NAD+. The structures reveal atomic-level details of the protein-binding interface, as well as unexpected NAD+-binding pockets within the interior of the vault cage. In addition, proteomics data show that human vaults purified from wild-type and PARP4-depleted cells interact with distinct subsets of proteins. Our results thereby support a model in which PARP4s specific incorporation into the vault cage helps to regulate vaults selection of cargo and its subcellular localization. Further, PARP4s proximity to MVPs NAD+-binding sites could support its enzymatic function within the vault.

biochemistry↗