scholarly journals NSUN6, an RNA methyltransferase of 5-mC controls glioblastoma response to Temozolomide (TMZ) via NELFB and RPS6KB2 interaction.

2021 ◽  
Author(s):  
Chidiebere U Awah ◽  
Jan Winter ◽  
Claudiane M Mazdoom ◽  
Olorunseun Ogunwobi

Nop2/Sun RNA methyltransferase (NSUN6) is an RNA 5 - methyl cytosine (5mC) transferase with little information known of its function in cancer and response to cancer therapy. Here, we show that NSUN6 methylates both large and small RNA in glioblastoma and controls glioblastoma response to temozolomide with or without influence of the MGMT promoter status, with high NSUN6 expression conferring survival benefit to glioblastoma patients and in other cancers. Mechanistically, our results show that NSUN6 controls response to TMZ therapy via 5mC mediated regulation of NELFB and RPS6BK2. Taken together, we present evidence that show that NSUN6 mediated 5mC deposition regulates transcriptional pause (by accumulation of NELFB and the general transcription factor complexes (POLR2A, TBP, TFIIA, TFIIE) on the preinitiation complex at TATA binding site to control translation machinery in glioblastoma response to alkylating agents. Our findings open a new frontier into controlling of transcriptional regulation by RNA methyltransferase and 5mC.

2013 ◽  
Vol 29 (9) ◽  
pp. 529-536 ◽  
Author(s):  
Guillermo Rodrigo ◽  
Thomas E. Landrain ◽  
Shensi Shen ◽  
Alfonso Jaramillo

2010 ◽  
Vol 30 (6) ◽  
pp. 1486-1494 ◽  
Author(s):  
Xianghua Piao ◽  
Xue Zhang ◽  
Ligang Wu ◽  
Joel G. Belasco

ABSTRACT MicroRNAs (miRNAs) repress gene expression posttranscriptionally by inhibiting translation and by expediting deadenylation so as to trigger rapid mRNA decay. Their regulatory influence is mediated by the protein components of the RNA-induced silencing complex (RISC), which deliver miRNAs and siRNAs to their mRNA targets. Here, we present evidence that CCR4-NOT is the deadenylase that removes poly(A) from messages destabilized by miRNAs in human cells. Overproducing a mutationally inactivated form of either of the catalytic subunits of this deadenylase (CCR4 or CAF1/POP2) significantly impedes the deadenylation and decay of mRNA targeted by a partially complementary miRNA. The same deadenylase initiates the degradation of “off-target” mRNAs that are bound by an imperfectly complementary siRNA introduced by transfection. The greater inhibitory effect of inactive CAF1 or POP2 (versus inactive CCR4) suggests a predominant role for this catalytic subunit of CCR4-NOT in miRNA- or small interfering RNA (siRNA)-mediated deadenylation. These effects of mi/siRNAs and CCR4-NOT can be fully reproduced by directly tethering RISC to mRNA without the guidance of a small RNA, indicating that the ability of RISC to accelerate deadenylation is independent of RNA base pairing. Despite its importance for mi/siRNA-mediated deadenylation, CCR4-NOT appears not to associate significantly with RISC, as judged by the failure of CAF1 and POP2 to coimmunoprecipitate detectably with either the Ago or TNRC6 subunit of RISC, a finding at odds with deadenylase recruitment as the mechanism by which RISC accelerates poly(A) removal.


2013 ◽  
Vol 8 (10) ◽  
pp. 1265-1284 ◽  
Author(s):  
Amrit S Boese ◽  
Anna Majer ◽  
Reuben Saba ◽  
Stephanie A Booth
Keyword(s):  

2008 ◽  
Vol 190 (11) ◽  
pp. 4075-4078 ◽  
Author(s):  
Roberto Balbontín ◽  
Nara Figueroa-Bossi ◽  
Josep Casadesús ◽  
Lionello Bossi

ABSTRACTInEscherichia coliandSalmonella enterica, RyeA and RyeB RNAs are encoded on opposite DNA strands at the same locus. We present evidence indicating that the last 23 bp of theryeBgene, corresponding to an internal portion of theryeAgene, served repeatedly as the integration site for exogenous DNA duringSalmonellaevolution and still act as an attachment site for present-day bacteriophages. Interestingly,ryeAsequence and expression are modified upon lysogenization.


2005 ◽  
Vol 173 (4S) ◽  
pp. 86-86
Author(s):  
Donna Y. Deng ◽  
Matthew P. Rutman ◽  
Larissa V. Rodriguez ◽  
Shlomo Raz
Keyword(s):  

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