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Rostam, N.

Publications and source records attributed to Rostam, N..

2 recordsLinked to original sources

PICNIC identifies condensate-forming proteins across organisms

Biomolecular condensates are membraneless organelles that can concentrate hundreds of different proteins to operate essential biological functions. However, accurate identification of their components remains challenging and biased towards proteins with high structural disorder content with focus on self-phase separating (driver) proteins. Here, we present a machine learning algorithm, PICNIC (Proteins Involved in CoNdensates In Cells) to classify proteins involved in biomolecular condensates regardless of their role in condensate formation. PICNIC successfully predicts condensate members by identifying amino acid patterns in the protein sequence and structure in addition to the intrinsic disorder and outperforms previous methods. We performed extensive experimental validation in cellulo and demonstrated that PICNIC accurately predicts 21 out of 24 condensate-forming proteins regardless of their structural disorder content. Even though increasing disorder content was associated with organismal complexity, we found no correlation between predicted condensate proteome content and disorder content across organisms. Overall, we applied a novel machine learning classifier to interrogate condensate components at single protein and whole-proteome levels across the tree of life (picnic.cd-code.org).

bioinformatics↗

Germ plasm anchors at tight junctions in the early zebrafish embryo

The zebrafish germline is specified during early embryogenesis by inherited maternal RNAs and proteins collectively called germ plasm. Only the cells containing germ plasm will become part of the germline, whereas other cells will commit to somatic cell fates. Therefore, proper localization of germ plasm is key for germ cell specification and its removal is critical for the development of soma. The molecular mechanism underlying this process in vertebrates is largely unknown. Here we show that germ plasm localization in zebrafish is similar to Xenopus and amniotes but distinct from Drosophila. We identified non muscle myosin II (NMII) and tight junction (TJ) components as interaction candidates of Bucky ball (Buc), which is the germ plasm organizer in zebrafish. Remarkably, we also found that TJ protein ZO1 colocalizes with germ plasm and electron microscopy (EM) of zebrafish embryos uncovered TJ like structures at early cleavage furrows. In addition, injection of the TJ-receptor Claudin-d (Cldn-d) produced extra germ plasm aggregates. Our findings discover for the first time a role of TJs in germ plasm localization.

developmental biology↗