-
Je něco špatně v tomto záznamu ?
In-depth analysis of cis-determinants that either promote or inhibit reinitiation on GCN4 mRNA after translation of its four short uORFs
S. Gunišová, P. Beznosková, MP. Mohammad, V. Vlčková, LS. Valášek,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1995 do Před 6 měsíci
PubMed Central
od 1995 do Před 1 rokem
Europe PubMed Central
od 1995 do Před 1 rokem
Open Access Digital Library
od 1995-03-01
PubMed
26822200
DOI
10.1261/rna.055046.115
Knihovny.cz E-zdroje
- MeSH
- iniciace translace peptidového řetězce MeSH
- messenger RNA genetika metabolismus MeSH
- otevřené čtecí rámce MeSH
- regulace genové exprese u hub MeSH
- Saccharomyces cerevisiae - proteiny genetika metabolismus MeSH
- Saccharomyces cerevisiae genetika metabolismus MeSH
- sekvence nukleotidů MeSH
- sekvenční analýza RNA MeSH
- transkripční faktory bZIP genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Translational control in eukaryotes is exerted by many means, one of which involves a ribosome translating multiple cistrons per mRNA as in bacteria. It is called reinitiation (REI) and occurs on mRNAs where the main ORF is preceded by a short upstream uORF(s). Some uORFs support efficient REI on downstream cistrons, whereas some others do not. The mRNA of yeast transcriptional activator GCN4 contains four uORFs of both types that together compose an intriguing regulatory mechanism of its expression responding to nutrients' availability and various stresses. Here we subjected all GCN4 uORFs to a comprehensive analysis to identify all REI-promoting and inhibiting cis-determinants that contribute either autonomously or in synergy to the overall efficiency of REI on GCN4. We found that the 3' sequences of uORFs 1-3 contain a conserved AU1-2A/UUAU2 motif that promotes REI in position-specific, autonomous fashion such as the REI-promoting elements occurring in 5' sequences of uORF1 and uORF2. We also identified autonomous and transferable REI-inhibiting elements in the 3' sequences of uORF2 and uORF3, immediately following their AU-rich motif. Furthermore, we analyzed contributions of coding triplets and terminating stop codon tetranucleotides of GCN4 uORFs showing a negative correlation between the efficiency of reinitiation and efficiency of translation termination. Together we provide a complex overview of all cis-determinants of REI with their effects set in the context of the overall GCN4 translational control.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16027709
- 003
- CZ-PrNML
- 005
- 20161031122658.0
- 007
- ta
- 008
- 161005s2016 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1261/rna.055046.115 $2 doi
- 024 7_
- $a 10.1261/rna.055046.115 $2 doi
- 035 __
- $a (PubMed)26822200
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Gunišová, Stanislava $u Laboratory of Regulation of Gene Expression, Institute of Microbiology AS CR, Prague 142 20, Czech Republic.
- 245 10
- $a In-depth analysis of cis-determinants that either promote or inhibit reinitiation on GCN4 mRNA after translation of its four short uORFs / $c S. Gunišová, P. Beznosková, MP. Mohammad, V. Vlčková, LS. Valášek,
- 520 9_
- $a Translational control in eukaryotes is exerted by many means, one of which involves a ribosome translating multiple cistrons per mRNA as in bacteria. It is called reinitiation (REI) and occurs on mRNAs where the main ORF is preceded by a short upstream uORF(s). Some uORFs support efficient REI on downstream cistrons, whereas some others do not. The mRNA of yeast transcriptional activator GCN4 contains four uORFs of both types that together compose an intriguing regulatory mechanism of its expression responding to nutrients' availability and various stresses. Here we subjected all GCN4 uORFs to a comprehensive analysis to identify all REI-promoting and inhibiting cis-determinants that contribute either autonomously or in synergy to the overall efficiency of REI on GCN4. We found that the 3' sequences of uORFs 1-3 contain a conserved AU1-2A/UUAU2 motif that promotes REI in position-specific, autonomous fashion such as the REI-promoting elements occurring in 5' sequences of uORF1 and uORF2. We also identified autonomous and transferable REI-inhibiting elements in the 3' sequences of uORF2 and uORF3, immediately following their AU-rich motif. Furthermore, we analyzed contributions of coding triplets and terminating stop codon tetranucleotides of GCN4 uORFs showing a negative correlation between the efficiency of reinitiation and efficiency of translation termination. Together we provide a complex overview of all cis-determinants of REI with their effects set in the context of the overall GCN4 translational control.
- 650 _2
- $a sekvence nukleotidů $7 D001483
- 650 _2
- $a transkripční faktory bZIP $x genetika $x metabolismus $7 D050976
- 650 _2
- $a regulace genové exprese u hub $7 D015966
- 650 _2
- $a otevřené čtecí rámce $7 D016366
- 650 _2
- $a iniciace translace peptidového řetězce $7 D010442
- 650 _2
- $a messenger RNA $x genetika $x metabolismus $7 D012333
- 650 _2
- $a Saccharomyces cerevisiae $x genetika $x metabolismus $7 D012441
- 650 _2
- $a Saccharomyces cerevisiae - proteiny $x genetika $x metabolismus $7 D029701
- 650 _2
- $a sekvenční analýza RNA $7 D017423
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Beznosková, Petra $u Laboratory of Regulation of Gene Expression, Institute of Microbiology AS CR, Prague 142 20, Czech Republic.
- 700 1_
- $a Mohammad, Mahabub Pasha $u Laboratory of Regulation of Gene Expression, Institute of Microbiology AS CR, Prague 142 20, Czech Republic.
- 700 1_
- $a Vlčková, Vladislava $u Laboratory of Regulation of Gene Expression, Institute of Microbiology AS CR, Prague 142 20, Czech Republic.
- 700 1_
- $a Valášek, Leoš Shivaya $u Laboratory of Regulation of Gene Expression, Institute of Microbiology AS CR, Prague 142 20, Czech Republic.
- 773 0_
- $w MED00006007 $t RNA (New York, N.Y.) $x 1469-9001 $g Roč. 22, č. 4 (2016), s. 542-58
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/26822200 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20161005 $b ABA008
- 991 __
- $a 20161031122622 $b ABA008
- 999 __
- $a ok $b bmc $g 1166023 $s 952339
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 22 $c 4 $d 542-58 $e 20160128 $i 1469-9001 $m RNA $n RNA $x MED00006007
- LZP __
- $a Pubmed-20161005