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dictyNews

Electronic Edition

Volume 45, number 21

August 23, 2019



Please submit abstracts of your papers as soon as they have been

accepted for publication by sending them to [log in to unmask]

or by using the form at

http://dictybase.org/db/cgi-bin/dictyBase/abstract_submit.



Back issues of dictyNews, the Dicty Reference database and other

useful information is available at dictyBase - http://dictybase.org.



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=========

Abstracts

=========





Microbiome management in the social amoeba Dictyostelium discoideum 

compared to humans (Review) 



Timothy Farinholt1, Christopher Dinh1,2, Adam Kuspa1,2

1Verna and Marrs McLean Department of Biochemistry and 

Molecular Biology, 

2Department of Molecular and Human Genetics, Baylor College of 

Medicine, Houston TX 77030.





Int J Dev Biol, Special Edition 

edited by Ricardo Escalante & Elena Cardenal, in press



Social amoebae and humans use common strategies to orchestrate 

their interactions with the bacteria in their respective environments and 

within their bodies. These strategies include the elimination of bacteria 

by phagocytosis, the establishment of mutualistic interactions, the 

elaboration of physical barriers, and the deployment of innate immune 

cells.  Many of the molecular mechanisms that humans and social 

amoebae employ differ, but there are striking similarities that may 

inform studies in each organism.  In this topical review we highlight the 

similarities and consider what we might learn by comparing these highly 

divergent species.  We focus on recent work in Dictyostelium discoideum 

with hopes of stimulating work in this area and with the expectation that 

new mechanistic details uncovered in social amoebae-bacteria 

interactions will inform microbiome management in humans.





submitted by:  Adam Kuspa [[log in to unmask]]

——————————————————————————————————————





[Auto]Biographical reflections on the contributions of William F. Loomis 

(1940-2016) to Dictyostelium biology.



Adam Kuspa1 and Gad Shaulsky2

1Verna and Marrs McLean Department of Biochemistry and 

Molecular Biology

2Department of Molecular and Human Genetics

Baylor College of Medicine, Houston, Texas USA 77030





Int J Dev Biol, Special Edition 

edited by Ricardo Escalante & Elena Cardenal, in press



William Farnsworth Loomis studied the social amoeba Dictyostelium 

discoideum for more than fifty years as a professor of biology at the 

University of California, San Diego.  This biographical reflection describes 

Dr. Loomis’ major scientific contributions to the field within a career arc

 that spanned the early days of molecular biology up to the present day 

 where the acquisition of high-dimensional datasets drive research.  

 Dr. Loomis explored the genetic control of social amoeba development, 

 delineated mechanisms of cell differentiation, as well as significantly 

 advancing genetic and genomic technology for the field.  The details of 

 Dr. Loomis’ multifaceted career are drawn from his published work, from 

 an autobiographical essay that he wrote near the end of his career and 

 from extensive conversations between him and the two authors, many 

 of which took place on the deck of his beachfront home in Del Mar, 

 California.





submitted by:  Adam Kuspa [[log in to unmask]]

——————————————————————————————————————





Dictyostelium discoideum and autophagy - a perfect pair



Sarah Fischer and Ludwig Eichinger



Centre for Biochemistry, Institute of Biochemistry I, Medical Faculty, 

University of Cologne, Cologne, Germany





Int J Dev Biol, Special Edition 

edited by Ricardo Escalante & Elena Cardenal, in press



Autophagy is subdivided into chaperone-mediated autophagy, 

microautophagy and macroautophagy and is a highly conserved 

intracellular degradative pathway. It is crucial for cellular homeostasis 

and also serves as a response to different stresses. Here we focus on 

macroautophagy, which targets damaged organelles, large protein 

assemblies as well as pathogenic intracellular microbes for destruction. 

During this process cytosolic material becomes enclosed in newly 

generated double-membrane vesicles, the so called autophagosomes. 

Upon maturation, the autophagosome fuses with the lysosome for 

degradation of the cargo. The basic molecular machinery that controls 

macroautophagy works in a sequential order and consists of the ATG1 

complex, the PtdIns3K complex, the membrane delivery system, two 

ubiquitin-like conjugation systems, and autophagy adaptors and 

receptors. Since the different stages of macroautophagy from initiation 

to final degradation of cargo are tightly regulated and highly conserved 

across eukaryotes, simple model organisms in combination with a 

wide range of techniques contributed significantly to advance our 

understanding of this complex dynamic process. Here, we present the 

social amoeba Dictyostelium discoideum as advantageous and relevant 

experimental model system for the analysis of macroautophagy.





submitted by:  Ludwig Eichinger [[log in to unmask]]

——————————————————————————————————————





Cellular allorecognition and its roles in Dictyostelium development and 

social evolution



Peter Kundert and Gad Shaulsky



Department of Molecular and Human Genetics, 

Baylor College of Medicine, Houston, TX 77030, USA



Int J Dev Biol, Special Edition 

edited by Ricardo Escalante & Elena Cardenal, in press



The social amoeba Dictyostelium discoideum is a tractable model 

organism to study cellular allorecognition, which is the ability of a cell to 

distinguish itself and its genetically similar relatives from more distantly 

related organisms. Cellular allorecognition is ubiquitous across the tree 

of life and affects many biological processes. Depending on the biological 

context, these versatile systems operate both within and between 

individual organisms, and both promote and constrain functional 

heterogeneity. Some of the most notable allorecognition systems mediate 

neural self-avoidance in flies and adaptive immunity in vertebrates. 

D. discoideum’s allorecognition system shares several structures and 

functions with other allorecognition systems. Structurally, its key 

regulators reside at a single genomic locus that encodes two highly 

polymorphic proteins, a transmembrane ligand called TgrC1 and its 

receptor TgrB1. These proteins exhibit isoform-specific, heterophilic 

binding across cells. Functionally, this interaction determines the extent 

to which co-developing D. discoideum strains co-aggregate or segregate 

during the aggregation phase of multicellular development. The 

allorecognition system thus affects both development and social 

evolution, as available evidence suggests that the threat of 

developmental cheating represents a primary selective force acting on 

it. Other significant characteristics that may inform the study of 

allorecognition in general include that D. discoideum’s allorecognition 

system is a continuous and inclusive trait, it is pleiotropic, and it is 

temporally regulated.





submitted by:  Gad Shaulsky [[log in to unmask]]

——————————————————————————————————————





scOrange—a tool for hands-on training of concepts from single-cell 

data analytics



Martin Stražar, Lan Žagar, Jaka Kokošar, Vesna Tanko, Aleš Erjavec, 

Pavlin G Poličar, Anže Starič, Janez Demšar, Gad Shaulsky, Vilas 

Menon, Andrew Lemire, Anup Parikh, and Blaž Zupan



Bioinformatics. 2019 Jul; 35(14): i4–i12.



Motivation

Single-cell RNA sequencing allows us to simultaneously profile the 

transcriptomes of thousands of cells and to indulge in exploring cell 

diversity, development and discovery of new molecular mechanisms. 

Analysis of scRNA data involves a combination of non-trivial steps from 

statistics, data visualization, bioinformatics and machine learning. 

Training molecular biologists in single-cell data analysis and empowering 

them to review and analyze their data can be challenging, both because 

of the complexity of the methods and the steep learning curve.



Results

We propose a workshop-style training in single-cell data analytics that 

relies on an explorative data analysis toolbox and a hands-on teaching 

style. The training relies on scOrange, a newly developed extension of 

a data mining framework that features workflow design through visual 

programming and interactive visualizations. Workshops with scOrange 

can proceed much faster than similar training methods that rely on 

computer programming and analysis through scripting in R or Python, 

allowing the trainer to cover more ground in the same time-frame. We 

here review the design principles of the scOrange toolbox that support 

such workshops and propose a syllabus for the course. We also provide 

examples of data analysis workflows that instructors can use during the 

training.



Availability and implementation

scOrange is an open-source software. The software, documentation and 

an emerging set of educational videos are available at http://singlecell.biolab.si.





submitted by:  Gad Shaulsky [[log in to unmask]]

——————————————————————————————————————





Democratized Image Analytics by Visual Programming through 

Integration of Deep Models and Small-Scale Machine Learning



Primož Godec, Matjaž Pančur, Nejc Ilenič, Andrejčopar, Martin Stražar, 

Aleš Erjavec, Ajda Pretnar, Janez Demšar, Anže Starič, Marko Toplak, 

Lan Žagar, Jan Hartman, Hamilton Wang, Riccardo Bellazzi, Uroš 

Petrovič, Silvia Garagna, Maurizio Zuccotti, Dongsu Park, Gad 

Shaulsky and Blaž Zupan





Nature Communications, accepted



Analysis of biomedical images requires computational expertise that are 

uncommon among biomedical scientists. Deep learning approaches for 

image analysis provide an opportunity to develop user-friendly tools for 

exploratory data analysis. Here, we use the visual programming toolbox 

Orange (http://orange.biolab.si) to simplify image analysis by integrating 

deep-learning embedding, machine learning procedures, and data 

visualization. Orange supports the construction of data analysis workflows 

by assembling components for data preprocessing, visualization, and 

modeling. We equipped Orange with components that use pre-trained 

deep convolutional networks to profile images with vectors of features. 

These vectors are used in image clustering and classification in a 

framework that enables mining of image sets for both novel and 

experienced users. We demonstrate the utility of the tool in image analysis 

of progenitor cells in mouse bone healing, identification of developmental 

competence in mouse oocytes, subcellular protein localization in yeast, 

and developmental morphology of social amoebae.





submitted by:  Gad Shaulsky [[log in to unmask]]

——————————————————————————————————————





The AK423 antibody recognizes Dictyostelium actin by Western blot



Wanessa Cristina Lima





Antibody Reports, 2019, vol. 2, e55

https://oap.unige.ch/journals/abrep/article/view/55



The AK423 antibody, derived from the 224-236-1 hybridoma, detects 

by Western blot the major actin protein from Dictyostelium discoideum. 

--------------------------------------------------------------------------------





The AK421 antibody recognizes the Dictyostelium mitochondrial porin 

by immunofluorescence



Wanessa Cristina Lima





Antibody Reports, 2019, vol. 2, e56

https://oap.unige.ch/journals/abrep/article/view/56



The AK421 antibody, derived from the 70-100-1 hybridoma, detects by 

immunofluorescence the mitochondrial porin from Dictyostelium discoideum. 

---------------------------------------------------------------------------------





The AK426 antibody recognizes the Golgi apparatus in Dictyostelium 

cells by immunofluorescence



Wanessa Cristina Lima



Antibody Reports, 2019, vol. 2, e59

https://oap.unige.ch/journals/abrep/article/view/59



The AK426 antibody, derived from the 1/39 hybridoma, detects by 

immunofluorescence the Golgi apparatus from Dictyostelium discoideum. 





submitted by: Wanessa Lima [[log in to unmask]]

==============================================================

[End dictyNews, volume 45, number 21]

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