The oxidoreductase PYROXD1 uses NAD(P)+ as an antioxidant to sustain tRNA ligase activity in pre-tRNA splicing and unfolded protein response

Igor Asanović; Emilia Strandback; Alena Kroupova; Djurdja Pasajlic; Anton Meinhart; Pai Tsung-Pin; Nemanja Djokovic; Dorothea Anrather; Thomas Schuetz; Marcin Józef Suskiewicz; Sirelin Sillamaa; Thomas Köcher; Rebecca Beveridge; Katarina Nikolic; Alexander Schleiffer; Martin Jinek; Markus Hartl; Tim Clausen; Josef Penninger; Peter Macheroux; Stefan Weitzer; Javier Martinez

doi:10.1016/j.molcel.2021.04.007

The oxidoreductase PYROXD1 uses NAD(P)+ as an antioxidant to sustain tRNA ligase activity in pre-tRNA splicing and unfolded protein response

Igor Asanović, Emilia Strandback, Alena Kroupova, Djurdja Pasajlic, Anton Meinhart, Pai Tsung-Pin, Nemanja Djokovic, Dorothea Anrather, Thomas Schuetz, Marcin Józef Suskiewicz, Sirelin Sillamaa, Thomas Köcher, Rebecca Beveridge, Katarina Nikolic, Alexander Schleiffer, Martin Jinek, Markus Hartl, Tim Clausen, Josef Penninger, Peter MacherouxStefan Weitzer^*, Javier Martinez^*

^*Corresponding author for this work

Institute of Biochemistry (6480)

Research output: Contribution to journal › Article › peer-review

Abstract

The tRNA ligase complex (tRNA-LC) splices precursor tRNAs (pre-tRNA), and Xbp1-mRNA during the unfolded protein response (UPR). In aerobic conditions, a cysteine residue bound to two metal ions in its ancient, catalytic subunit RTCB could make the tRNA-LC susceptible to oxidative inactivation. Here, we confirm this hypothesis and reveal a co-evolutionary association between the tRNA-LC and PYROXD1, a conserved and essential oxidoreductase. We reveal that PYROXD1 preserves the activity of the mammalian tRNA-LC in pre-tRNA splicing and UPR. PYROXD1 binds the tRNA-LC in the presence of NAD(P)H and converts RTCB-bound NAD(P)H into NAD(P)+, a typical oxidative co-enzyme. However, NAD(P)+ here acts as an antioxidant and protects the tRNA-LC from oxidative inactivation, which is dependent on copper ions. Genetic variants of PYROXD1 that cause human myopathies only partially support tRNA-LC activity. Thus, we establish the tRNA-LC as an oxidation-sensitive metalloenzyme, safeguarded by the flavoprotein PYROXD1 through an unexpected redox mechanism.

Original language	English
Pages (from-to)	2520-2532.e16
Number of pages	13
Journal	Molecular Cell
Volume	81
Issue number	12
DOIs	https://doi.org/10.1016/j.molcel.2021.04.007
Publication status	Published - 17 Jun 2021

Keywords

copper
metalloenzyme
myopathy
NADH
NADPH
oxidative stress
oxidoreductase
pre-tRNA splicing
PYROXD1
RtcB
tRNA ligase complex
UPR

ASJC Scopus subject areas

Molecular Biology
Cell Biology

Fields of Expertise

Human- & Biotechnology

Access to Document

10.1016/j.molcel.2021.04.007

Cite this

Asanović, I., Strandback, E., Kroupova, A., Pasajlic, D., Meinhart, A., Tsung-Pin, P., Djokovic, N., Anrather, D., Schuetz, T., Suskiewicz, M. J., Sillamaa, S., Köcher, T., Beveridge, R., Nikolic, K., Schleiffer, A., Jinek, M., Hartl, M., Clausen, T., Penninger, J., ... Martinez, J. (2021). The oxidoreductase PYROXD1 uses NAD(P)+ as an antioxidant to sustain tRNA ligase activity in pre-tRNA splicing and unfolded protein response. Molecular Cell, 81(12), 2520-2532.e16. https://doi.org/10.1016/j.molcel.2021.04.007

Asanović, I, Strandback, E, Kroupova, A, Pasajlic, D, Meinhart, A, Tsung-Pin, P, Djokovic, N, Anrather, D, Schuetz, T, Suskiewicz, MJ, Sillamaa, S, Köcher, T, Beveridge, R, Nikolic, K, Schleiffer, A, Jinek, M, Hartl, M, Clausen, T, Penninger, J, Macheroux, P, Weitzer, S & Martinez, J 2021, 'The oxidoreductase PYROXD1 uses NAD(P)+ as an antioxidant to sustain tRNA ligase activity in pre-tRNA splicing and unfolded protein response', Molecular Cell, vol. 81, no. 12, pp. 2520-2532.e16. https://doi.org/10.1016/j.molcel.2021.04.007

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title = "The oxidoreductase PYROXD1 uses NAD(P)+ as an antioxidant to sustain tRNA ligase activity in pre-tRNA splicing and unfolded protein response",

abstract = "The tRNA ligase complex (tRNA-LC) splices precursor tRNAs (pre-tRNA), and Xbp1-mRNA during the unfolded protein response (UPR). In aerobic conditions, a cysteine residue bound to two metal ions in its ancient, catalytic subunit RTCB could make the tRNA-LC susceptible to oxidative inactivation. Here, we confirm this hypothesis and reveal a co-evolutionary association between the tRNA-LC and PYROXD1, a conserved and essential oxidoreductase. We reveal that PYROXD1 preserves the activity of the mammalian tRNA-LC in pre-tRNA splicing and UPR. PYROXD1 binds the tRNA-LC in the presence of NAD(P)H and converts RTCB-bound NAD(P)H into NAD(P)+, a typical oxidative co-enzyme. However, NAD(P)+ here acts as an antioxidant and protects the tRNA-LC from oxidative inactivation, which is dependent on copper ions. Genetic variants of PYROXD1 that cause human myopathies only partially support tRNA-LC activity. Thus, we establish the tRNA-LC as an oxidation-sensitive metalloenzyme, safeguarded by the flavoprotein PYROXD1 through an unexpected redox mechanism.",

keywords = "copper, metalloenzyme, myopathy, NADH, NADPH, oxidative stress, oxidoreductase, pre-tRNA splicing, PYROXD1, RtcB, tRNA ligase complex, UPR",

author = "Igor Asanovi{\'c} and Emilia Strandback and Alena Kroupova and Djurdja Pasajlic and Anton Meinhart and Pai Tsung-Pin and Nemanja Djokovic and Dorothea Anrather and Thomas Schuetz and Suskiewicz, {Marcin J{\'o}zef} and Sirelin Sillamaa and Thomas K{\"o}cher and Rebecca Beveridge and Katarina Nikolic and Alexander Schleiffer and Martin Jinek and Markus Hartl and Tim Clausen and Josef Penninger and Peter Macheroux and Stefan Weitzer and Javier Martinez",

year = "2021",

month = jun,

day = "17",

doi = "10.1016/j.molcel.2021.04.007",

language = "English",

volume = "81",

pages = "2520--2532.e16",

journal = "Molecular Cell",

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number = "12",

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T1 - The oxidoreductase PYROXD1 uses NAD(P)+ as an antioxidant to sustain tRNA ligase activity in pre-tRNA splicing and unfolded protein response

AU - Asanović, Igor

AU - Strandback, Emilia

AU - Kroupova, Alena

AU - Pasajlic, Djurdja

AU - Meinhart, Anton

AU - Tsung-Pin, Pai

AU - Djokovic, Nemanja

AU - Anrather, Dorothea

AU - Schuetz, Thomas

AU - Suskiewicz, Marcin Józef

AU - Sillamaa, Sirelin

AU - Köcher, Thomas

AU - Beveridge, Rebecca

AU - Nikolic, Katarina

AU - Schleiffer, Alexander

AU - Jinek, Martin

AU - Hartl, Markus

AU - Clausen, Tim

AU - Penninger, Josef

AU - Macheroux, Peter

AU - Weitzer, Stefan

AU - Martinez, Javier

PY - 2021/6/17

Y1 - 2021/6/17

N2 - The tRNA ligase complex (tRNA-LC) splices precursor tRNAs (pre-tRNA), and Xbp1-mRNA during the unfolded protein response (UPR). In aerobic conditions, a cysteine residue bound to two metal ions in its ancient, catalytic subunit RTCB could make the tRNA-LC susceptible to oxidative inactivation. Here, we confirm this hypothesis and reveal a co-evolutionary association between the tRNA-LC and PYROXD1, a conserved and essential oxidoreductase. We reveal that PYROXD1 preserves the activity of the mammalian tRNA-LC in pre-tRNA splicing and UPR. PYROXD1 binds the tRNA-LC in the presence of NAD(P)H and converts RTCB-bound NAD(P)H into NAD(P)+, a typical oxidative co-enzyme. However, NAD(P)+ here acts as an antioxidant and protects the tRNA-LC from oxidative inactivation, which is dependent on copper ions. Genetic variants of PYROXD1 that cause human myopathies only partially support tRNA-LC activity. Thus, we establish the tRNA-LC as an oxidation-sensitive metalloenzyme, safeguarded by the flavoprotein PYROXD1 through an unexpected redox mechanism.

AB - The tRNA ligase complex (tRNA-LC) splices precursor tRNAs (pre-tRNA), and Xbp1-mRNA during the unfolded protein response (UPR). In aerobic conditions, a cysteine residue bound to two metal ions in its ancient, catalytic subunit RTCB could make the tRNA-LC susceptible to oxidative inactivation. Here, we confirm this hypothesis and reveal a co-evolutionary association between the tRNA-LC and PYROXD1, a conserved and essential oxidoreductase. We reveal that PYROXD1 preserves the activity of the mammalian tRNA-LC in pre-tRNA splicing and UPR. PYROXD1 binds the tRNA-LC in the presence of NAD(P)H and converts RTCB-bound NAD(P)H into NAD(P)+, a typical oxidative co-enzyme. However, NAD(P)+ here acts as an antioxidant and protects the tRNA-LC from oxidative inactivation, which is dependent on copper ions. Genetic variants of PYROXD1 that cause human myopathies only partially support tRNA-LC activity. Thus, we establish the tRNA-LC as an oxidation-sensitive metalloenzyme, safeguarded by the flavoprotein PYROXD1 through an unexpected redox mechanism.

KW - copper

KW - metalloenzyme

KW - myopathy

KW - NADH

KW - NADPH

KW - oxidative stress

KW - oxidoreductase

KW - pre-tRNA splicing

KW - PYROXD1

KW - RtcB

KW - tRNA ligase complex

KW - UPR

UR - http://www.scopus.com/inward/record.url?scp=85107908607&partnerID=8YFLogxK

U2 - 10.1016/j.molcel.2021.04.007

DO - 10.1016/j.molcel.2021.04.007

M3 - Article

C2 - 33930333

SN - 1097-2765

VL - 81

SP - 2520-2532.e16

JO - Molecular Cell

JF - Molecular Cell

IS - 12

ER -

The oxidoreductase PYROXD1 uses NAD(P)+ as an antioxidant to sustain tRNA ligase activity in pre-tRNA splicing and unfolded protein response

Abstract

Keywords

ASJC Scopus subject areas

Fields of Expertise

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