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Dictybase Northwestern <[log in to unmask]>
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Fri, 30 Jan 2015 22:00:56 +0000
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dictyNews
Electronic Edition
Volume 41, number 3
January 30, 2015

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
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=========
Abstracts
=========

Comparative genome and transcriptome analyses of the social amoeba 
Acytostelium subglobosum that accomplishes multicellular development 
without germ-soma differentiation.

Hideko Urushihara, Hidekazu Kuwayama, Kensuke Fukuhara, Takehiko 
Itoh, Hiroshi Kagoshima, Tadasu Shin-I, Atsushi Toyoda, Kazuyo 
Ohishi, Tateaki Taniguchi, Hideki Noguchi, Yoko Kuroki, Takashi 
Hata, Kyoko Uchi, Kurato Mohri, Jason S. King, Robert H. Insall, 
Yuji Kohara, Asao Fujiyama.


BMC Genomics, in press.

Background: Social amoebae are lower eukaryotes that inhabit the 
soil. They are characterized by the construction of a starvation-
induced multicellular fruiting body with a spore ball and 
supportive stalk. In most species, the stalk is filled with motile 
stalk cells, as represented by the model organism Dictyostelium 
discoideum, whose developmental mechanisms have been well 
characterized. However, in the genus Acytostelium, the stalk is 
acellular and all aggregated cells become spores. Phylogenetic 
analyses have shown that it is not an ancestral genus but has 
lost the ability to undergo cell differentiation.

Results: We performed genome and transcriptome analyses of 
Acytostelium subglobosum and compared our findings to other 
available dictyostelid genome data. Although A. subglobosum 
adopts a qualitatively different developmental program from other 
dictyostelids, its gene repertoire was largely conserved. Yet, 
families of polyketide synthase and extracellular matrix proteins 
have not expanded and a serine protease and ABC transporter B 
family gene, tagA, and a few other developmental genes are missing 
in the A. subglobosum lineage. Temporal gene expression patterns 
are astonishingly dissimilar from those of D. discoideum, and only 
a limited fraction of the ortholog pairs shared the same expression 
patterns, so that some signaling cascades for development seem to 
be disabled in A. subglobosum.

Conclusions: The absence of the ability to undergo cell 
differentiation in Acytostelium is accompanied by a small change 
in coding potential and extensive alterations in gene expression 
patterns.


Submitted by Hideko Urushihara [[log in to unmask]] 
----------------------------------------------------------------------


A Long-range Foresight for the Medical Application of Apoptosis 
Specifically Induced by Dd-MRP4, Dictyostelium Mitochondrial 
Ribosomal Protein S4, to Cancer Therapy

Yasuo Maeda

Department of Developmental Biology and Neurosciences , 
Graduate School of Life Sciences, Tohoku University (Emeritus), 
Aoba, Sendai 980-8578, Japan; E-mail: [log in to unmask]


Biomolecules, in press

Apoptosis (programmed cell death) is regarded as ultimate 
differentiation of the cell. We have recently demonstrated that 
a targeted delivery of Dd-MRP4 (Dictyostelium mitochondrial 
ribosomal protein S4) suppresses specifically the proliferation 
of the human cancer cells, by inducing their apoptotic cell 
death [1]. This amazing fact was discovered, simply based on the 
finding that Dd-MRP4 expression is absolutely required for 
transition of Dictyostelium cells from growth to differentiation 
[2,3]. Dd-MRP4 protein has quite unique structural characters, in 
that it is highly basic (pI: about 11.5) and interestingly has 
several nuclear-localization signals within the molecule. In this 
review, we introduce briefly the efficacy of several apoptosis-
inducing substances reported thus far for cancer therapy, and 
speculate the possible mechanisms, by which apoptosis is 
specifically induced by Dd-MRP4, on the basis of its structural 
uniqueness. We also discuss about several issues to be solved for 
the medical application of ectopically expressed Dd-MRP4 in human 
cancer cells.

Keywords: apoptosis; cell differentiation; cancer therapy; Dd-MRP4 
(Dictyostelium mitochondrial ribosomal protein S4); microRNA 
(miRNA); mitochondria; Dictyostelim discoideum; human cancer 
cells

(References)
1.	Chida, J.; Araki, H.; Maeda Y. Specific growth suppression 
of human cancer cells by targeted delivery of Dictyostelium 
mitochondrial ribosomal protein S4. Cancer Cell International 
2014, 14:56.
2.	Chida, J.; Amagai, A.; Tanaka, M.; Maeda Y. Establishment 
of a new method for precisely determining the functions of 
individual mitochondrial genes using Dictyostelium cells. 
BMC Genet. 2008, 9:.doi:10.1186/1471-2156-9-25.
3.	Maeda, Y.; Chida, J. Control of cell differentiation by 
mitochondria, typically evidenced in Dictyostelium development. 
Biomolecules 2013, 3, 943-966; doi:10.3390/biom3040943.


Submitted by Yasuo Maeda [[log in to unmask]]   
==============================================================
[End dictyNews, volume 41, number 3]

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