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A list by Prachee Avasthi Recommended Reading
See what researchers at Prachee Avasthi’s lab are reading to discover some interesting new work.
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The actin assembly requirements of the formin Fus1 to build the fusion focus
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
This is a great demonstration (using chimeras of formin FH2 and FH1 domains from a diverse range of formins) that tuning the actin nucleation and elongation rates of formins affects actin architecture. This can help explain how various cell types can generate unique actin structures optimized for a particular function as in this case for Fus1’s role in assembling the structure required for fusion of fission yeast cells during mating.
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Vimentin intermediate filaments organize organellar architecture in response to ER stress
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
Interesting function of intermediate filaments though an ER embedded protein: this protein, a ubiquitin ligase, links the perinuclear ER with vimentin-based intermediate filaments for ER and stress-dependent endosome positioning. The work was done in U2OS cells.
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High-resolution secretory timeline from vesicle formation at the Golgi to fusion at the plasma membrane in S. cerevisiae
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
This is a must-read spatio-temporal characterization of secretory pathway events during yeast exocytosis. This will undoubtedly impact our thinking about secretory traffic during processes like encystment and ciliogenesis across a range of unicellular eukaryotes.
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Imaging tools generated by CRISPR/Cas9 tagging reveal cytokinetic diversity in mammalian cells
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
This paper is a good reminder of the heterogeneity in phenotypes that can be observed when visualizing molecular players at physiological levels.
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Atypical small GTPase RABL3 interacts with RAB11 to regulate early ciliogenesis in human cells
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
A new GTPase player in ciliogenesis in human (RPE1) cells binds directly to rab11 and is needed for ciliary vesicle formation.
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Identifying the genes impacted by cell proliferation in proteomics and transcriptomics studies
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
Interesting framing…identifying genes that are robustly correlated with cell proliferation not to find novel mechanisms of division but to eliminate confounding contributions of cell proliferation in cellular processes analyzed by large data sets.
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Alterations to the broad-spectrum formin inhibitor SMIFH2 improve potency
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
Thanks to @cdmacquarrie for alerting me to this one! Synthesis of SMIFH2 derivatives identifies more potent versions (5-fold decrease in IC50) that are able to inhibit all human formins. This increased potency may reduce off target inhibition of myosins at higher concentrations. Myosins aren’t directly tested in this study.
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Transient accumulation and bidirectional movement of KIF13B in primary cilia
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
Worm cilia are perhaps not as unique as we thought. A kinesin-3 accumulates in a subset of cilia in human cultured cells and undergoes bursts of bidirectional motor domain dependent movement.
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The dynamics of protein localisation to restricted zones within Drosophila mechanosensory cilia
This article's authorsAnnotation by Prachee Avasthi Recommended Reading
Very interesting study tackling the sub-compartmentalization of cilia. In fly chorodonal neurons, cilia have differences in outer and inner dynein arm complexes along the apical-distal axis of the axoneme. This paper highlights different modes of establishing this subcompartmentalization whether by restriction to proximal regions (ODAs) or by uniform localization and maturation to final proximal restriction (IDAs). Access to the axonemal interior, binding affinities via docking complexes, tubulin modification and pruning of IDA localization by retrograde IFT-mediated removal are suggested as possible factors.
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Moving Yeasts: Resolving the Mystery
This article's authors