-
Something wrong with this record ?
Cell Distribution within Yeast Colonies and Colony Biofilms: How Structure Develops
V. Plocek, L. Váchová, V. Šťovíček, Z. Palková
Language English Country Switzerland
Document type Journal Article
Grant support
19-11384S
Czech Science Foundation
LQ1604 NPU II
MEYS
RVO 61388971
Czech Academy of Sciences
BIOCEV CZ.1.05/1.1.00/02.0109
ERDF and MEYS
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
32485964
DOI
10.3390/ijms21113873
Knihovny.cz E-resources
- MeSH
- Biofilms * MeSH
- Cell Division MeSH
- Membrane Glycoproteins genetics metabolism MeSH
- Microbial Interactions MeSH
- Mutation MeSH
- Saccharomyces cerevisiae Proteins genetics metabolism MeSH
- Saccharomyces cerevisiae cytology metabolism physiology MeSH
- Publication type
- Journal Article MeSH
Multicellular structures formed by yeasts and other microbes are valuable models for investigating the processes of cell-cell interaction and pattern formation, as well as cell signaling and differentiation. These processes are essential for the organization and development of diverse microbial communities that are important in everyday life. Two major types of multicellular structures are formed by yeast Saccharomyces cerevisiae on semisolid agar. These are colonies formed by laboratory or domesticated strains and structured colony biofilms formed by wild strains. These structures differ in spatiotemporal organization and cellular differentiation. Using state-of-the-art microscopy and mutant analysis, we investigated the distribution of cells within colonies and colony biofilms and the involvement of specific processes therein. We show that prominent differences between colony and biofilm structure are determined during early stages of development and are associated with the different distribution of growing cells. Two distinct cell distribution patterns were identified-the zebra-type and the leopard-type, which are genetically determined. The role of Flo11p in cell adhesion and extracellular matrix production is essential for leopard-type distribution, because FLO11 deletion triggers the switch to zebra-type cell distribution. However, both types of cell organization are independent of cell budding polarity and cell separation as determined using respective mutants.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc21012561
- 003
- CZ-PrNML
- 005
- 20210507102607.0
- 007
- ta
- 008
- 210420s2020 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/ijms21113873 $2 doi
- 035 __
- $a (PubMed)32485964
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Plocek, Vítězslav $u Department of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 12800 Prague, Czech Republic
- 245 10
- $a Cell Distribution within Yeast Colonies and Colony Biofilms: How Structure Develops / $c V. Plocek, L. Váchová, V. Šťovíček, Z. Palková
- 520 9_
- $a Multicellular structures formed by yeasts and other microbes are valuable models for investigating the processes of cell-cell interaction and pattern formation, as well as cell signaling and differentiation. These processes are essential for the organization and development of diverse microbial communities that are important in everyday life. Two major types of multicellular structures are formed by yeast Saccharomyces cerevisiae on semisolid agar. These are colonies formed by laboratory or domesticated strains and structured colony biofilms formed by wild strains. These structures differ in spatiotemporal organization and cellular differentiation. Using state-of-the-art microscopy and mutant analysis, we investigated the distribution of cells within colonies and colony biofilms and the involvement of specific processes therein. We show that prominent differences between colony and biofilm structure are determined during early stages of development and are associated with the different distribution of growing cells. Two distinct cell distribution patterns were identified-the zebra-type and the leopard-type, which are genetically determined. The role of Flo11p in cell adhesion and extracellular matrix production is essential for leopard-type distribution, because FLO11 deletion triggers the switch to zebra-type cell distribution. However, both types of cell organization are independent of cell budding polarity and cell separation as determined using respective mutants.
- 650 12
- $a biofilmy $7 D018441
- 650 _2
- $a buněčné dělení $7 D002455
- 650 _2
- $a membránové glykoproteiny $x genetika $x metabolismus $7 D008562
- 650 _2
- $a mikrobiální interakce $7 D056265
- 650 _2
- $a mutace $7 D009154
- 650 _2
- $a Saccharomyces cerevisiae $x cytologie $x metabolismus $x fyziologie $7 D012441
- 650 _2
- $a Saccharomyces cerevisiae - proteiny $x genetika $x metabolismus $7 D029701
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Váchová, Libuše $u Institute of Microbiology of the Czech Academy of Sciences, BIOCEV, 14220 Prague, Czech Republic
- 700 1_
- $a Šťovíček, Vratislav $u Department of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 12800 Prague, Czech Republic
- 700 1_
- $a Palková, Zdena $u Department of Genetics and Microbiology, Faculty of Science, Charles University, BIOCEV, 12800 Prague, Czech Republic
- 773 0_
- $w MED00176142 $t International journal of molecular sciences $x 1422-0067 $g Roč. 21, č. 11 (2020)
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/32485964 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20210420 $b ABA008
- 991 __
- $a 20210507102607 $b ABA008
- 999 __
- $a ok $b bmc $g 1650847 $s 1132940
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2020 $b 21 $c 11 $e 20200529 $i 1422-0067 $m International journal of molecular sciences $n Int J Mol Sci $x MED00176142
- GRA __
- $a 19-11384S $p Czech Science Foundation
- GRA __
- $a LQ1604 NPU II $p MEYS
- GRA __
- $a RVO 61388971 $p Czech Academy of Sciences
- GRA __
- $a BIOCEV CZ.1.05/1.1.00/02.0109 $p ERDF and MEYS
- LZP __
- $a Pubmed-20210420