Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Knockdown of the Ribosomal Protein eL29 in Mammalian Cells Leads to Significant Changes in Gene Expression at the Transcription Level. / Gopanenko, Alexander V.; Kolobova, Alena V.; Meschaninova, Maria I. и др.
в: Cells, Том 9, № 5, 1228, 15.05.2020.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Knockdown of the Ribosomal Protein eL29 in Mammalian Cells Leads to Significant Changes in Gene Expression at the Transcription Level
AU - Gopanenko, Alexander V.
AU - Kolobova, Alena V.
AU - Meschaninova, Maria I.
AU - Venyaminova, Alya G.
AU - Tupikin, Alexey E.
AU - Kabilov, Marsel R.
AU - Malygin, Alexey A.
AU - Karpova, Galina G.
PY - 2020/5/15
Y1 - 2020/5/15
N2 - An imbalance in the synthesis of ribosomal proteins can lead to the disruption of various cellular processes. For mammalian cells, it has been shown that the level of the eukaryote-specific ribosomal protein eL29, also known as the one interacting with heparin/heparan sulfate, substantially affects their growth. Moreover, in animals lacking this protein, a number of anatomical abnormalities have been observed. Here, we applied next-generation RNA sequencing to HEK293 cells transfected with siRNAs specific for the mRNA of eL29 to determine what changes occur in the transcriptome profile with a decrease in the level of the target protein. We showed that an approximately 2.5-fold decrease in the content of eL29 leads to statistically significant changes in the expression of more than a thousand genes at the transcription level, without a noticeable effect on cell viability, rRNA level, and global translation. The set of eL29-dependent genes included both up-regulated and down-regulated ones, among which there are those previously identified as targets for proteins implicated in oncogenesis. Thus, our findings demonstrate that an insufficiency of eL29 in mammalian cells causes a significant reorganization of gene expression, thereby highlighting the relationship between the cellular balance of eL29 and the activities of certain genes.
AB - An imbalance in the synthesis of ribosomal proteins can lead to the disruption of various cellular processes. For mammalian cells, it has been shown that the level of the eukaryote-specific ribosomal protein eL29, also known as the one interacting with heparin/heparan sulfate, substantially affects their growth. Moreover, in animals lacking this protein, a number of anatomical abnormalities have been observed. Here, we applied next-generation RNA sequencing to HEK293 cells transfected with siRNAs specific for the mRNA of eL29 to determine what changes occur in the transcriptome profile with a decrease in the level of the target protein. We showed that an approximately 2.5-fold decrease in the content of eL29 leads to statistically significant changes in the expression of more than a thousand genes at the transcription level, without a noticeable effect on cell viability, rRNA level, and global translation. The set of eL29-dependent genes included both up-regulated and down-regulated ones, among which there are those previously identified as targets for proteins implicated in oncogenesis. Thus, our findings demonstrate that an insufficiency of eL29 in mammalian cells causes a significant reorganization of gene expression, thereby highlighting the relationship between the cellular balance of eL29 and the activities of certain genes.
KW - differential gene expression
KW - eL29-dependent genes
KW - eL29-related processes
KW - HEK293 cells
KW - knockdown of ribosomal protein eL29
KW - next-generation sequencing
KW - RNA-seq
KW - SULFATE-BINDING
KW - RNA
KW - TRANSLATION
KW - MATURATION
KW - SACCHAROMYCES-CEREVISIAE
KW - COLLAGEN-XXIV
KW - REGULATOR
KW - LACKING
KW - GROWTH
KW - RPL29
UR - http://www.scopus.com/inward/record.url?scp=85084964475&partnerID=8YFLogxK
U2 - 10.3390/cells9051228
DO - 10.3390/cells9051228
M3 - Article
C2 - 32429214
AN - SCOPUS:85084964475
VL - 9
JO - Cells
JF - Cells
SN - 2073-4409
IS - 5
M1 - 1228
ER -
ID: 24330508