PRMT5 methylome profiling uncovers a direct link to splicing regulation in acute myeloid leukemia

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

PRMT5 methylome profiling uncovers a direct link to splicing regulation in acute myeloid leukemia. / Radzisheuskaya, Aliaksandra; Shliaha, Pavel V; Grinev, Vasily; Lorenzini, Eugenia; Kovalchuk, Sergey; Shlyueva, Daria; Gorshkov, Vladimir; Hendrickson, Ronald C; Jensen, Ole N; Helin, Kristian.

In: Nature Structural & Molecular Biology, Vol. 26, No. 11, 2019, p. 999-1012.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Radzisheuskaya, A, Shliaha, PV, Grinev, V, Lorenzini, E, Kovalchuk, S, Shlyueva, D, Gorshkov, V, Hendrickson, RC, Jensen, ON & Helin, K 2019, 'PRMT5 methylome profiling uncovers a direct link to splicing regulation in acute myeloid leukemia', Nature Structural & Molecular Biology, vol. 26, no. 11, pp. 999-1012. https://doi.org/10.1038/s41594-019-0313-z

APA

Radzisheuskaya, A., Shliaha, P. V., Grinev, V., Lorenzini, E., Kovalchuk, S., Shlyueva, D., Gorshkov, V., Hendrickson, R. C., Jensen, O. N., & Helin, K. (2019). PRMT5 methylome profiling uncovers a direct link to splicing regulation in acute myeloid leukemia. Nature Structural & Molecular Biology, 26(11), 999-1012. https://doi.org/10.1038/s41594-019-0313-z

Vancouver

Radzisheuskaya A, Shliaha PV, Grinev V, Lorenzini E, Kovalchuk S, Shlyueva D et al. PRMT5 methylome profiling uncovers a direct link to splicing regulation in acute myeloid leukemia. Nature Structural & Molecular Biology. 2019;26(11):999-1012. https://doi.org/10.1038/s41594-019-0313-z

Author

Radzisheuskaya, Aliaksandra ; Shliaha, Pavel V ; Grinev, Vasily ; Lorenzini, Eugenia ; Kovalchuk, Sergey ; Shlyueva, Daria ; Gorshkov, Vladimir ; Hendrickson, Ronald C ; Jensen, Ole N ; Helin, Kristian. / PRMT5 methylome profiling uncovers a direct link to splicing regulation in acute myeloid leukemia. In: Nature Structural & Molecular Biology. 2019 ; Vol. 26, No. 11. pp. 999-1012.

Bibtex

@article{ecc54d0c0a67478e971949cc3c128dad,
title = "PRMT5 methylome profiling uncovers a direct link to splicing regulation in acute myeloid leukemia",
abstract = "Protein arginine methyltransferase 5 (PRMT5) has emerged as a promising cancer drug target, and three PRMT5 inhibitors are currently in clinical trials for multiple malignancies. In this study, we investigated the role of PRMT5 in human acute myeloid leukemia (AML). Using an enzymatic dead version of PRMT5 and a PRMT5-specific inhibitor, we demonstrated the requirement of the catalytic activity of PRMT5 for the survival of AML cells. We then identified PRMT5 substrates using multiplexed quantitative proteomics and investigated their role in the survival of AML cells. We found that the function of the splicing regulator SRSF1 relies on its methylation by PRMT5 and that loss of PRMT5 leads to changes in alternative splicing of multiple essential genes. Our study proposes a mechanism for the requirement of PRMT5 for leukemia cell survival and provides potential biomarkers for the treatment response to PRMT5 inhibitors.",
author = "Aliaksandra Radzisheuskaya and Shliaha, {Pavel V} and Vasily Grinev and Eugenia Lorenzini and Sergey Kovalchuk and Daria Shlyueva and Vladimir Gorshkov and Hendrickson, {Ronald C} and Jensen, {Ole N} and Kristian Helin",
year = "2019",
doi = "10.1038/s41594-019-0313-z",
language = "English",
volume = "26",
pages = "999--1012",
journal = "Nature Structural and Molecular Biology",
issn = "1545-9993",
publisher = "nature publishing group",
number = "11",

}

RIS

TY - JOUR

T1 - PRMT5 methylome profiling uncovers a direct link to splicing regulation in acute myeloid leukemia

AU - Radzisheuskaya, Aliaksandra

AU - Shliaha, Pavel V

AU - Grinev, Vasily

AU - Lorenzini, Eugenia

AU - Kovalchuk, Sergey

AU - Shlyueva, Daria

AU - Gorshkov, Vladimir

AU - Hendrickson, Ronald C

AU - Jensen, Ole N

AU - Helin, Kristian

PY - 2019

Y1 - 2019

N2 - Protein arginine methyltransferase 5 (PRMT5) has emerged as a promising cancer drug target, and three PRMT5 inhibitors are currently in clinical trials for multiple malignancies. In this study, we investigated the role of PRMT5 in human acute myeloid leukemia (AML). Using an enzymatic dead version of PRMT5 and a PRMT5-specific inhibitor, we demonstrated the requirement of the catalytic activity of PRMT5 for the survival of AML cells. We then identified PRMT5 substrates using multiplexed quantitative proteomics and investigated their role in the survival of AML cells. We found that the function of the splicing regulator SRSF1 relies on its methylation by PRMT5 and that loss of PRMT5 leads to changes in alternative splicing of multiple essential genes. Our study proposes a mechanism for the requirement of PRMT5 for leukemia cell survival and provides potential biomarkers for the treatment response to PRMT5 inhibitors.

AB - Protein arginine methyltransferase 5 (PRMT5) has emerged as a promising cancer drug target, and three PRMT5 inhibitors are currently in clinical trials for multiple malignancies. In this study, we investigated the role of PRMT5 in human acute myeloid leukemia (AML). Using an enzymatic dead version of PRMT5 and a PRMT5-specific inhibitor, we demonstrated the requirement of the catalytic activity of PRMT5 for the survival of AML cells. We then identified PRMT5 substrates using multiplexed quantitative proteomics and investigated their role in the survival of AML cells. We found that the function of the splicing regulator SRSF1 relies on its methylation by PRMT5 and that loss of PRMT5 leads to changes in alternative splicing of multiple essential genes. Our study proposes a mechanism for the requirement of PRMT5 for leukemia cell survival and provides potential biomarkers for the treatment response to PRMT5 inhibitors.

U2 - 10.1038/s41594-019-0313-z

DO - 10.1038/s41594-019-0313-z

M3 - Journal article

C2 - 31611688

VL - 26

SP - 999

EP - 1012

JO - Nature Structural and Molecular Biology

JF - Nature Structural and Molecular Biology

SN - 1545-9993

IS - 11

ER -

ID: 229305635