dictyNews
Electronic Edition
Volume 47, number 14
June 25, 2021
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Abstracts
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Transcriptional milestones in Dictyostelium development
Mariko Katoh-Kurasawa, Karin Hrovatin, Shigenori Hirose,
Amanda Webb, Hsing-I Ho, Blaž Zupan and Gad Shaulsky
Department of Molecular and Human Genetics, Baylor College of
Medicine, Houston, TX, 77030 USA
Faculty of Computer and Information Science, University of
Ljubljana, SI-1000 Ljubljana, Slovenia
Genome Research, accepted
The manuscript is available at
https://www.biorxiv.org/content/10.1101/2021.05.27.445976v1
and the data are available for exploration on dictyExpress.
Dictyostelium development begins with single-cell starvation
and ends with multicellular fruiting bodies. Developmental
morphogenesis is accompanied by sweeping transcriptional
changes, encompassing nearly half of the 13,000 genes in the
genome. We performed time-series RNA-sequencing analyses of
the wild type and 20 mutants to explore the relationships between
transcription and morphogenesis,. These strains exhibit
developmental arrest at different stages, accelerated development,
or atypical morphologies. Considering eight major morphological
transitions, we identified 1,371 milestone genes whose expression
changes sharply between consecutive transitions. We also identified
1,099 genes as members of 21 regulons, which are groups of genes
that remain coordinately regulated despite the genetic, temporal,
and developmental perturbations. The gene annotations in these
groups validate known transitions and reveal new developmental
events. For example, DNA replication genes are tightly co-regulated
with cell division genes, so they are expressed in mid-development
even though chromosomal DNA is not replicated. Our dataset
includes 486 transcriptional profiles that can help identify new
relationships between transcription and development and improve
gene annotations. We demonstrate its utility by showing that cycles
of aggregation and disaggregation in allorecognition-defective
mutants involve dedifferentiation. We also show sensitivity to
genetic and developmental conditions in two commonly used actin
genes, act6 and act15, and robustness of the coaA gene. Finally,
we propose that gpdA is a better mRNA quantitation standard
because it is less sensitive to external conditions than commonly
used standards. The dataset is available for democratized
exploration through the web application dictyExpress and the
data mining environment Orange.
submitted by: Gad Shaulsky [[log in to unmask]]
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Macropinocytosis: biology and mechanisms
Robert R. Kay
MRC Laboratory of Molecular Biology Francis Crick Avenue
Cambridge CB2 0QH, UK
Cells & Development, in press
Macropinocytosis is a form of endocytosis performed by ruffles and
cups of the plasma membrane. These close to entrap droplets of
medium into micron-sized vesicles, which are trafficked through the
endocytic system, their contents digested and useful products
absorbed. Macropinocytosis is constitutive in certain immune cells
and stimulated in many other cells by growth factors. It occurs
across the animal kingdom and in amoebae, implying a deep
evolutionary history. Its scientific history goes back 100 years, but
increasingly work is focused on its medical importance in the immune
system, cancer cell feeding, and as a backdoor into cells for viruses
and drugs. Macropinocytosis is driven by the actin cytoskeleton whose
dynamics can be appreciated with lattice light sheet microscopy: this
revealsa surprising variety of routes for forming macropinosomes. In
Dictyostelium amoebae, macropinocytic cups are organized around
domains of PIP3 and active Ras and Rac in the plasma membrane.
These attract activators of the Arp2/3 complex to their periphery,
creating rings of actin polymerization that shape the cups. The size
of PIP3 domains is by RasGAPs, such as NF1, and the lipid
phosphatase, PTEN. It is likely that domain dynamics determine
the shape, evolution and closing of macropinocytic structures.
submitted by: Rob Kay [[log in to unmask]]
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