The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i<

Maintaining translation fidelity is a critical step within the process of gene expression. It requires the involvement of numerous regulatory elements to ensure the synthesis of functional proteins. The efficient termination of protein synthesis can play a crucial role in preserving this fidelity. H...
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Autor*in:	Sarah Takallou [verfasserIn] Maryam Hajikarimlou [verfasserIn] Mustafa Al-gafari [verfasserIn] Jiashu Wang [verfasserIn] Thomas David Daniel Kazmirchuk [verfasserIn] Kamaledin B. Said [verfasserIn] Bahram Samanfar [verfasserIn] Ashkan Golshani [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2024

Schlagwörter:	gene expression codon protein synthesis premature stop codon yeast

Übergeordnetes Werk:	In: Biology - MDPI AG, 2012, 13(2024), 3, p 138
Übergeordnetes Werk:	volume:13 ; year:2024 ; number:3, p 138

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.3390/biology13030138

Katalog-ID:	DOAJ100549756

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allfieldsSound	10.3390/biology13030138 doi (DE-627)DOAJ100549756 (DE-599)DOAJbf80d5ab9dfd4381aba179e71c29a083 DE-627 ger DE-627 rakwb eng QH301-705.5 Sarah Takallou verfasserin aut The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i< 2024 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Maintaining translation fidelity is a critical step within the process of gene expression. It requires the involvement of numerous regulatory elements to ensure the synthesis of functional proteins. The efficient termination of protein synthesis can play a crucial role in preserving this fidelity. Here, we report on investigating a protein of unknown function, <i<YNR069C</i< (also known as <i<BSC5</i<), for its activity in the process of translation. We observed a significant increase in the bypass of premature stop codons upon the deletion of <i<YNR069C</i<. Interestingly, the genomic arrangement of this ORF suggests a compatible mode of expression reliant on translational readthrough, incorporating the neighboring open reading frame. We also showed that the deletion of <i<YNR069C</i< results in an increase in the rate of translation. Based on our results, we propose that <i<YNR069C</i< may play a role in translation fidelity, impacting the overall quantity and quality of translation. Our genetic interaction analysis supports our hypothesis, associating the role of <i<YNR069C</i< to the regulation of protein synthesis. gene expression codon protein synthesis premature stop codon yeast Biology (General) Maryam Hajikarimlou verfasserin aut Mustafa Al-gafari verfasserin aut Jiashu Wang verfasserin aut Thomas David Daniel Kazmirchuk verfasserin aut Kamaledin B. Said verfasserin aut Bahram Samanfar verfasserin aut Ashkan Golshani verfasserin aut In Biology MDPI AG, 2012 13(2024), 3, p 138 (DE-627)718622073 (DE-600)2661517-4 20797737 nnns volume:13 year:2024 number:3, p 138 https://doi.org/10.3390/biology13030138 kostenfrei https://doaj.org/article/bf80d5ab9dfd4381aba179e71c29a083 kostenfrei https://www.mdpi.com/2079-7737/13/3/138 kostenfrei https://doaj.org/toc/2079-7737 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2024 3, p 138
language	English
source	In Biology 13(2024), 3, p 138 volume:13 year:2024 number:3, p 138
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authorswithroles_txt_mv	Sarah Takallou @@aut@@ Maryam Hajikarimlou @@aut@@ Mustafa Al-gafari @@aut@@ Jiashu Wang @@aut@@ Thomas David Daniel Kazmirchuk @@aut@@ Kamaledin B. Said @@aut@@ Bahram Samanfar @@aut@@ Ashkan Golshani @@aut@@
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callnumber-first	Q - Science
author	Sarah Takallou
spellingShingle	Sarah Takallou misc QH301-705.5 misc gene expression misc codon misc protein synthesis misc premature stop codon misc yeast misc Biology (General) The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i<
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topic_title	QH301-705.5 The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i< gene expression codon protein synthesis premature stop codon yeast
topic	misc QH301-705.5 misc gene expression misc codon misc protein synthesis misc premature stop codon misc yeast misc Biology (General)
topic_unstemmed	misc QH301-705.5 misc gene expression misc codon misc protein synthesis misc premature stop codon misc yeast misc Biology (General)
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title	The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i<
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title_full	The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i<
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author_browse	Sarah Takallou Maryam Hajikarimlou Mustafa Al-gafari Jiashu Wang Thomas David Daniel Kazmirchuk Kamaledin B. Said Bahram Samanfar Ashkan Golshani
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title_auth	The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i<
abstract	Maintaining translation fidelity is a critical step within the process of gene expression. It requires the involvement of numerous regulatory elements to ensure the synthesis of functional proteins. The efficient termination of protein synthesis can play a crucial role in preserving this fidelity. Here, we report on investigating a protein of unknown function, <i<YNR069C</i< (also known as <i<BSC5</i<), for its activity in the process of translation. We observed a significant increase in the bypass of premature stop codons upon the deletion of <i<YNR069C</i<. Interestingly, the genomic arrangement of this ORF suggests a compatible mode of expression reliant on translational readthrough, incorporating the neighboring open reading frame. We also showed that the deletion of <i<YNR069C</i< results in an increase in the rate of translation. Based on our results, we propose that <i<YNR069C</i< may play a role in translation fidelity, impacting the overall quantity and quality of translation. Our genetic interaction analysis supports our hypothesis, associating the role of <i<YNR069C</i< to the regulation of protein synthesis.
abstractGer	Maintaining translation fidelity is a critical step within the process of gene expression. It requires the involvement of numerous regulatory elements to ensure the synthesis of functional proteins. The efficient termination of protein synthesis can play a crucial role in preserving this fidelity. Here, we report on investigating a protein of unknown function, <i<YNR069C</i< (also known as <i<BSC5</i<), for its activity in the process of translation. We observed a significant increase in the bypass of premature stop codons upon the deletion of <i<YNR069C</i<. Interestingly, the genomic arrangement of this ORF suggests a compatible mode of expression reliant on translational readthrough, incorporating the neighboring open reading frame. We also showed that the deletion of <i<YNR069C</i< results in an increase in the rate of translation. Based on our results, we propose that <i<YNR069C</i< may play a role in translation fidelity, impacting the overall quantity and quality of translation. Our genetic interaction analysis supports our hypothesis, associating the role of <i<YNR069C</i< to the regulation of protein synthesis.
abstract_unstemmed	Maintaining translation fidelity is a critical step within the process of gene expression. It requires the involvement of numerous regulatory elements to ensure the synthesis of functional proteins. The efficient termination of protein synthesis can play a crucial role in preserving this fidelity. Here, we report on investigating a protein of unknown function, <i<YNR069C</i< (also known as <i<BSC5</i<), for its activity in the process of translation. We observed a significant increase in the bypass of premature stop codons upon the deletion of <i<YNR069C</i<. Interestingly, the genomic arrangement of this ORF suggests a compatible mode of expression reliant on translational readthrough, incorporating the neighboring open reading frame. We also showed that the deletion of <i<YNR069C</i< results in an increase in the rate of translation. Based on our results, we propose that <i<YNR069C</i< may play a role in translation fidelity, impacting the overall quantity and quality of translation. Our genetic interaction analysis supports our hypothesis, associating the role of <i<YNR069C</i< to the regulation of protein synthesis.
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title_short	The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i<
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The Involvement of <i<YNR069C</i< in Protein Synthesis in the Baker’s Yeast, <i<Saccharomyces cerevisiae</i<

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