-
Je něco špatně v tomto záznamu ?
Arginine methylation augments Sbp1 function in translation repression and decapping
N. Bhatter, R. Roy, S. Shah, SP. Sastry, S. Parbin, R. Iyappan, S. Kankaria, PI. Rajyaguru,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
Wellcome Trust - United Kingdom
IA/I/12/2/500625
DBT-Wellcome Trust India Alliance - India
IA/I/12/2/500625
Wellcome DBT India Alliance - International
BT/PR13267/BRB/10/1444/2015
Department of Biotechnology, India - International
NLK
Free Medical Journals
od 2005 do Před 1 rokem
Medline Complete (EBSCOhost)
od 2005-01-01 do Před 1 rokem
Wiley Free Content
od 2005 do Před 1 rokem
PubMed
31495062
DOI
10.1111/febs.15057
Knihovny.cz E-zdroje
- MeSH
- aminokyselinové motivy MeSH
- arginin metabolismus MeSH
- cirkulární dichroismus MeSH
- cytoplazmatická granula metabolismus MeSH
- messenger RNA metabolismus MeSH
- metylace MeSH
- posttranslační úpravy proteinů MeSH
- proteiny vázající selen metabolismus MeSH
- Saccharomyces cerevisiae - proteiny metabolismus MeSH
- sekvence aminokyselin MeSH
- vazba proteinů MeSH
- western blotting MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The fate of messenger RNA in cytoplasm plays a crucial role in various cellular processes. However, the mechanisms that decide whether mRNA will be translated, degraded or stored remain unclear. Single stranded nucleic acid binding protein (Sbp1), an Arginine-Glycine-Glycine (RGG-motif) protein, is known to promote transition of mRNA into a repressed state by binding eukaryotic translation initiation factor 4G1 (eIF4G1) and to promote mRNA decapping, perhaps by modulation of Dcp1/2 activity. Sbp1 is known to be methylated on arginine residues in RGG-motif; however, the functional relevance of this modification in vivo remains unknown. Here, we report that Sbp1 is arginine-methylated in an hnRNP methyl transferase (Hmt1)-dependent manner and that methylation is enhanced upon glucose deprivation. Characterization of an arginine-methylation-defective (AMD) mutant provided evidence that methylation affects Sbp1 function in vivo. The AMD mutant is compromised in causing growth defect upon overexpression, and the mutant is defective in both localizing to and inducing granule formation. Importantly, the Sbp1-eIF4G1 interaction is compromised both for the AMD mutant and in the absence of Hmt1. Upon overexpression, wild-type Sbp1 increases localization of another RGG motif containing protein, Scd6 (suppressor of clathrin deficiency) to granules; however, this property of Sbp1 is compromised in the AMD mutant and in the absence of Hmt1, indicating that Sbp1 repression activity could involve other RGG-motif translation repressors. Additionally, the AMD mutant fails to increase localization of the decapping activator DEAD box helicase homolog to foci and fails to rescue the decapping defect of a dcp1-2Δski8 strain, highlighting the role of Sbp1 methylation in decapping. Taken together, these results suggest that arginine methylation modulates Sbp1 role in mRNA fate determination.
Department of Biochemistry Indian Institute of Science Bangalore India
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc20023389
- 003
- CZ-PrNML
- 005
- 20201214125918.0
- 007
- ta
- 008
- 201125s2019 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1111/febs.15057 $2 doi
- 035 __
- $a (PubMed)31495062
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Bhatter, Nupur $u Department of Biochemistry, Indian Institute of Science, Bangalore, India.
- 245 10
- $a Arginine methylation augments Sbp1 function in translation repression and decapping / $c N. Bhatter, R. Roy, S. Shah, SP. Sastry, S. Parbin, R. Iyappan, S. Kankaria, PI. Rajyaguru,
- 520 9_
- $a The fate of messenger RNA in cytoplasm plays a crucial role in various cellular processes. However, the mechanisms that decide whether mRNA will be translated, degraded or stored remain unclear. Single stranded nucleic acid binding protein (Sbp1), an Arginine-Glycine-Glycine (RGG-motif) protein, is known to promote transition of mRNA into a repressed state by binding eukaryotic translation initiation factor 4G1 (eIF4G1) and to promote mRNA decapping, perhaps by modulation of Dcp1/2 activity. Sbp1 is known to be methylated on arginine residues in RGG-motif; however, the functional relevance of this modification in vivo remains unknown. Here, we report that Sbp1 is arginine-methylated in an hnRNP methyl transferase (Hmt1)-dependent manner and that methylation is enhanced upon glucose deprivation. Characterization of an arginine-methylation-defective (AMD) mutant provided evidence that methylation affects Sbp1 function in vivo. The AMD mutant is compromised in causing growth defect upon overexpression, and the mutant is defective in both localizing to and inducing granule formation. Importantly, the Sbp1-eIF4G1 interaction is compromised both for the AMD mutant and in the absence of Hmt1. Upon overexpression, wild-type Sbp1 increases localization of another RGG motif containing protein, Scd6 (suppressor of clathrin deficiency) to granules; however, this property of Sbp1 is compromised in the AMD mutant and in the absence of Hmt1, indicating that Sbp1 repression activity could involve other RGG-motif translation repressors. Additionally, the AMD mutant fails to increase localization of the decapping activator DEAD box helicase homolog to foci and fails to rescue the decapping defect of a dcp1-2Δski8 strain, highlighting the role of Sbp1 methylation in decapping. Taken together, these results suggest that arginine methylation modulates Sbp1 role in mRNA fate determination.
- 650 _2
- $a aminokyselinové motivy $7 D020816
- 650 _2
- $a sekvence aminokyselin $7 D000595
- 650 _2
- $a arginin $x metabolismus $7 D001120
- 650 _2
- $a western blotting $7 D015153
- 650 _2
- $a cirkulární dichroismus $7 D002942
- 650 _2
- $a cytoplazmatická granula $x metabolismus $7 D003594
- 650 _2
- $a metylace $7 D008745
- 650 _2
- $a vazba proteinů $7 D011485
- 650 _2
- $a posttranslační úpravy proteinů $7 D011499
- 650 _2
- $a messenger RNA $x metabolismus $7 D012333
- 650 _2
- $a Saccharomyces cerevisiae - proteiny $x metabolismus $7 D029701
- 650 _2
- $a proteiny vázající selen $x metabolismus $7 D051137
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Roy, Raju $u Department of Biochemistry, Indian Institute of Science, Bangalore, India.
- 700 1_
- $a Shah, Shanaya $u University of California, Davis, CA, USA.
- 700 1_
- $a Sastry, Sneha P $u Department of Biochemistry, Indian Institute of Science, Bangalore, India.
- 700 1_
- $a Parbin, Sabnam $u Department of Biochemistry, Indian Institute of Science, Bangalore, India.
- 700 1_
- $a Iyappan, Rajan $u IAPG Academy of Science, Libechov, Czech Republic.
- 700 1_
- $a Kankaria, Siddharth $u Department of Biochemistry, Indian Institute of Science, Bangalore, India.
- 700 1_
- $a Rajyaguru, Purusharth I $u Department of Biochemistry, Indian Institute of Science, Bangalore, India.
- 773 0_
- $w MED00008414 $t The FEBS journal $x 1742-4658 $g Roč. 286, č. 23 (2019), s. 4693-4708
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/31495062 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20201125 $b ABA008
- 991 __
- $a 20201214125917 $b ABA008
- 999 __
- $a ok $b bmc $g 1595708 $s 1114065
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 286 $c 23 $d 4693-4708 $e 20190923 $i 1742-4658 $m The FEBS journal $n FEBS J $x MED00008414
- GRA __
- $p Wellcome Trust $2 United Kingdom
- GRA __
- $a IA/I/12/2/500625 $p DBT-Wellcome Trust India Alliance $2 India
- GRA __
- $a IA/I/12/2/500625 $p Wellcome DBT India Alliance $2 International
- GRA __
- $a BT/PR13267/BRB/10/1444/2015 $p Department of Biotechnology, India $2 International
- LZP __
- $a Pubmed-20201125