Nudt21 regulates the alternative polyadenylation of Pak1 and is predictive in the prognosis of glioblastoma patients
Alternative polyadenylation (APA) has emerged as a prevalent feature associated with cancer development and progression. The advantage of APA to tumor progression is to induce oncogenes through 3′-UTR shortening, and to inactivate tumor suppressor genes via the re-routing of microRNA competition. We...
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Published in | Oncogene Vol. 38; no. 21; pp. 4154 - 4168 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.05.2019
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Alternative polyadenylation (APA) has emerged as a prevalent feature associated with cancer development and progression. The advantage of APA to tumor progression is to induce oncogenes through 3′-UTR shortening, and to inactivate tumor suppressor genes via the re-routing of microRNA competition. We previously identified the Mammalian Cleavage Factor I-25 (CFIm25) (encoded by
Nudt21
gene
)
as a master APA regulator whose expression levels directly impact the tumorigenicity of glioblastoma (GBM) in vitro and in vivo. Despite its importance, the role of
Nudt21
in GBM development is not known and the genes subject to
Nudt21
APA regulation that contribute to GBM progression have not been identified. Here, we find that
Nudt21
is reduced in low grade glioma (LGG) and all four subtypes of high grade glioma (GBM). Reduced expression of
Nudt21
associates with worse survival in TCGA LGG cohorts and two TCGA GBM cohorts. Moreover, although CFIm25 was initially identified as biochemically associated with both CFIm59 and CFIm68, we observed three CFIm distinct subcomplexes exist and CFIm59 protein level is dependent on
Nudt21
expression in GBM cells, but CFIm68 is not, and that only
CFIm59
predicts prognosis of GBM patients similar to
Nudt21
. Through the use of Poly(A)-Click-Seq to characterize APA, we define the mRNAs subject to 3′-UTR shortening upon
Nudt21
depletion in GBM cells and observed enrichment in genes important in the
Ras
signaling pathway, including
Pak1
. Remarkably, we find that
Pak1
expression is regulated by
Nudt21
through its 3′-UTR APA, and the combination of
Pak1
and
Nudt21
expression generates an even stronger prognostic indicator of GBM survival versus either value used alone. Collectively, our data uncover
Nudt21
and its downstream target
Pak1
as a potential “combination biomarker” for predicting prognosis of GBM patients. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Author contributions E.J.W and P.J. conceived the project, designed the experiments and Y.C. and N.E. performed the experiments and data analysis. C.W. and Z.X. performed survival analysis. N.E. and A. R. performed the PAC-Seq APA analysis. L.L. and W.L. performed TCGA GBM RNA-seq data analysis, T.C. helped with data analysis. Y.C., P.J., and E.J.W. wrote the manuscript with input from N.E., L.L., T.C., and A.R. |
ISSN: | 0950-9232 1476-5594 1476-5594 |
DOI: | 10.1038/s41388-019-0714-9 |