The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation

<strong>Background:</strong> X chromosome inactivation in mammals is regulated by the non-coding (nc) RNA, Xist, which represses the chromosome from which it is transcribed. High levels of the N6-methyladenosine (m6A) RNA modification occur within Xist exon I, close to the 5’ end of the...

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Main Authors: Coker, H, Wei, G, Moindrot, B, Mohammed, S, Nesterova, T, Brockdorff, N
Format: Journal article
Language:English
Published: F1000Research 2020
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author Coker, H
Wei, G
Moindrot, B
Mohammed, S
Nesterova, T
Brockdorff, N
author_facet Coker, H
Wei, G
Moindrot, B
Mohammed, S
Nesterova, T
Brockdorff, N
author_sort Coker, H
collection OXFORD
description <strong>Background:</strong> X chromosome inactivation in mammals is regulated by the non-coding (nc) RNA, Xist, which represses the chromosome from which it is transcribed. High levels of the N6-methyladenosine (m6A) RNA modification occur within Xist exon I, close to the 5’ end of the transcript, and also further 3’, in Xist exon VII. The m6A modification is catalysed by the METTL3/14 complex that is directed to specific targets, including Xist, by the RNA binding protein RBM15/15B. m6A modification of Xist RNA has been reported to be important for Xist–mediated gene silencing. <br> <strong>Methods:</strong> We use CRISPR/Cas9 mediated mutagenesis to delete sequences around the 5’ m6A region in interspecific XX mouse embryonic stem cells (mESCs). Following induction of Xist RNA expression, we assay chromosome silencing using allelic RNA-seq and Xist m6A distribution using m6A-seq. Additionally, we use Xist RNA FISH to analyse the effect of deleting the 5’ m6A region on the function of the endogenous Xist promoter. We purify epitope tagged RBM15 from mESCs, and then apply MS/MS analysis to define the RBM15 interactome. <br> <strong>Results:</strong> We show that a deletion encompassing the entire Xist 5’ m6A region results in a modest reduction in Xist-mediated silencing, and that the 5’ m6A region overlaps essential DNA elements required for activation of the endogenous Xist promoter. Deletion of the Xist A-repeat, to which RBM15 binds, entirely abolishes deposition of m6A in the Xist 5’ m6A region without affecting the modification in exon VII. We show that in mESCs, RBM15 interacts with the m6A complex, the SETD1B histone modifying complex, and several proteins linked to RNA metabolism. <br> <strong>Conclusions:</strong> Our findings support that RBM15 binding to the Xist A-repeat recruits the m6A complex to the 5’ Xist m6A region and that this region plays a role in Xist-mediated chromosome silencing.
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spelling oxford-uuid:d0ee4304-2114-49e5-b8ae-3b6cebd1d8fd2022-03-27T07:53:37ZThe role of the Xist 5' m6A region and RBM15 in X chromosome inactivationJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:d0ee4304-2114-49e5-b8ae-3b6cebd1d8fdEnglishSymplectic ElementsF1000Research2020Coker, HWei, GMoindrot, BMohammed, SNesterova, TBrockdorff, N<strong>Background:</strong> X chromosome inactivation in mammals is regulated by the non-coding (nc) RNA, Xist, which represses the chromosome from which it is transcribed. High levels of the N6-methyladenosine (m6A) RNA modification occur within Xist exon I, close to the 5’ end of the transcript, and also further 3’, in Xist exon VII. The m6A modification is catalysed by the METTL3/14 complex that is directed to specific targets, including Xist, by the RNA binding protein RBM15/15B. m6A modification of Xist RNA has been reported to be important for Xist–mediated gene silencing. <br> <strong>Methods:</strong> We use CRISPR/Cas9 mediated mutagenesis to delete sequences around the 5’ m6A region in interspecific XX mouse embryonic stem cells (mESCs). Following induction of Xist RNA expression, we assay chromosome silencing using allelic RNA-seq and Xist m6A distribution using m6A-seq. Additionally, we use Xist RNA FISH to analyse the effect of deleting the 5’ m6A region on the function of the endogenous Xist promoter. We purify epitope tagged RBM15 from mESCs, and then apply MS/MS analysis to define the RBM15 interactome. <br> <strong>Results:</strong> We show that a deletion encompassing the entire Xist 5’ m6A region results in a modest reduction in Xist-mediated silencing, and that the 5’ m6A region overlaps essential DNA elements required for activation of the endogenous Xist promoter. Deletion of the Xist A-repeat, to which RBM15 binds, entirely abolishes deposition of m6A in the Xist 5’ m6A region without affecting the modification in exon VII. We show that in mESCs, RBM15 interacts with the m6A complex, the SETD1B histone modifying complex, and several proteins linked to RNA metabolism. <br> <strong>Conclusions:</strong> Our findings support that RBM15 binding to the Xist A-repeat recruits the m6A complex to the 5’ Xist m6A region and that this region plays a role in Xist-mediated chromosome silencing.
spellingShingle Coker, H
Wei, G
Moindrot, B
Mohammed, S
Nesterova, T
Brockdorff, N
The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation
title The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation
title_full The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation
title_fullStr The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation
title_full_unstemmed The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation
title_short The role of the Xist 5' m6A region and RBM15 in X chromosome inactivation
title_sort role of the xist 5 m6a region and rbm15 in x chromosome inactivation
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