dc.contributor |
Roberto Sánchez Olea;0000-0002-6523-7821 |
es_MX |
dc.contributor.advisor |
Sáncez Olea, Roberto |
|
dc.contributor.advisor |
Calera Medina, Mónica Raquel |
|
dc.contributor.advisor |
Riego Ruiz, Lina Raquel |
|
dc.contributor.advisor |
Layseca Espinosa, Esther |
|
dc.contributor.advisor |
Salgado Bustamante, Mariana |
|
dc.contributor.author |
Mora García, Martín Antonio |
|
dc.coverage.spatial |
México. San Luis Potosí. San Luis Potosí. |
es_MX |
dc.creator |
Martín Antonio Mora García;781284 |
es_MX |
dc.date.accessioned |
2022-11-03T18:58:06Z |
|
dc.date.available |
2023-11-09 |
|
dc.date.available |
2022-11-03T18:58:06Z |
|
dc.date.issued |
2022-11-09 |
|
dc.identifier.uri |
https://repositorioinstitucional.uaslp.mx/xmlui/handle/i/8053 |
|
dc.description.abstract |
The GPN-loop GTPase Npa3 is encoded by an essential gene in the yeast Saccharomyces cerevisiae. Npa3 plays a critical role in the assembly and nuclear accumulation of RNA polymerase II (RNAPII), a function that may explain its essentiality. Genetic interactions describe the extent to which a mutation in a particular gene affects a specific phenotype when co-occurring with an alteration in a second gene. Discovering synthetic negative genetic interactions has long been used as a tool to delineate the functional relatedness between pairs of genes participating in common or compensatory biological pathways. Previously, our group showed that nuclear targeting and transcriptional activity of RNAPII were unaffected in cells expressing exclusively a C-terminal truncated mutant version of Npa3 (npa3ΔC) lacking the last 106-residues naturally absent from the single GPN protein in Archaea, but universally conserved in all Npa3 orthologs of eukaryotes. In order to gain insight into novel cellular functions for Npa3, we performed here a genome-wide Synthetic Genetic Array (SGA) study coupled to bulk fluorescence monitoring to identify negative genetic interactions of NPA3 by crossing an npa3ΔC strain with a 4,389-nonessential gene-deletion collection. This genetic screen revealed previously unknown synthetic negative interactions between NPA3 and 15 genes. Our results revealed that the Npa3 C-terminal tail extension regulates the participation of this essential GTPase in previously unknown biological processes related to mitochondrial homeostasis and ribosome biogenesis. |
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dc.description.statementofresponsibility |
Investigadores |
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dc.description.statementofresponsibility |
Estudiantes |
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dc.language |
Inglés |
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dc.publisher |
Facultad de Medicina |
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dc.rights |
Acceso Embargado |
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dc.rights.uri |
http://creativecommons.org/licenses/by-nc-nd/4.0 |
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dc.subject |
GTPase Npa3 |
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dc.subject |
C-terminal deleted Npa3 |
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dc.subject |
Gpn1 |
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dc.subject |
synthetic genetic interactions |
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dc.subject |
synthetic lethal |
es_MX |
dc.subject |
fluorescence |
es_MX |
dc.subject |
mitochondria |
es_MX |
dc.subject |
ribosome biogenesis |
es_MX |
dc.subject.other |
BIOLOGÍA Y QUIMICA |
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dc.subject.other |
MEDICINA Y CIENCIAS DE LA SALUD |
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dc.title |
Función de la GTPasa Npa3 en la levadura Saccharomyces cerevisiae |
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dc.type |
Tesis de doctorado |
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dc.degree.name |
Doctorado en Ciencias Biomédicas Básicas |
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dc.degree.department |
Facultad de Medicina |
es_MX |