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Biology subjects

Gerstner, M.

Publications and source records attributed to Gerstner, M..

2 recordsLinked to original sources

A revised genome annotation of the model cyanobacterium Synechocystis based on start and stop codon-enriched ribosome profiling and proteogenomics

Cyanobacteria are important primary producers and are used as microbial cell factories due to their ability to use solar light for oxygenic photosynthesis. Synechocystis sp. PCC 6803 is a popular model cyanobacterium, yet there are ambiguities in the precise coding regions of many genes, and numerous genes encoding small proteins have remained undetected. Here we present the results of a riboproteogenomic analysis, combining ribosome profiling (Ribo-seq) analysis involving inhibitors that stall ribosomes at translation initiation and termination sites (TIS- and TTS-Ribo-seq), with a proteogenomic reevaluation and reannotation of its entire genome. We report evidence for the translation of 3,055 annotated genes based on proteogenomics (83%), of 3,492 based on Ribo-seq (95.2%), and of 3,018 supported by both methods (82%). The data suggested unannotated protein-coding genes and corrections for annotated ones. We validated 15 small proteins translated from antisense RNAs, from intergenic and intragenic regions and provide proteogenomic support for up to 69 further, mostly small proteins. With slr0489, slr1079 and slr1082 we identified three genes with intragenic out-of-frame translons and show that both the internal and host reading frames are translated and that the resulting proteins interact with each other. Our data can be accessed via an intuitive and interactive genome browser platform at https://www.bioinf.uni-freiburg.de/[~]ribobase/. They illustrate the enormous value of consolidating genome annotations in the context of integrated experimental data.

microbiology↗

Glypican-1 drives unconventional secretion of Fibroblast Growth Factor 2

Fibroblast Growth Factor 2 (FGF2) is a tumor cell survival factor that is transported into the extracellular space by an unconventional secretory mechanism. Cell surface heparan sulfate proteoglycans are known to play an essential role in this process. Unexpectedly, we found that among the diverse sub-classes consisting of syndecans, perlecans, glypicans and others, Glypican-1 (GPC1) is both the principle and rate-limiting factor that drives unconventional secretion of FGF2. By contrast, we demonstrate GPC1 to be dispensable for FGF2 signaling into cells. We provide first insights into the structural basis for GPC1-dependent FGF2 secretion, identifying disaccharides with N-linked sulfate groups to be enriched in the heparan sulfate chains of GPC1 to which FGF2 binds with high affinity. Our findings have broad implications for the role of GPC1 as a key molecule in tumor progression.

biochemistry↗