Spen links RNA-mediated endogenous retrovirus silencing and X chromosome inactivation

Author:

Carter Ava C1ORCID,Xu Jin1ORCID,Nakamoto Meagan Y2,Wei Yuning1,Zarnegar Brian J3,Shi Quanming1,Broughton James P1,Ransom Ryan C4,Salhotra Ankit4,Nagaraja Surya D5,Li Rui1,Dou Diana R1ORCID,Yost Kathryn E1,Cho Seung-Woo1,Mistry Anil6,Longaker Michael T45,Khavari Paul A3,Batey Robert T2,Wuttke Deborah S2,Chang Howard Y137ORCID

Affiliation:

1. Center for Personal Dynamic Regulomes, Stanford University, Stanford, United States

2. Department of Biochemistry, University of Colorado, Boulder, United States

3. Department of Dermatology, Stanford University School of Medicine, Stanford, United States

4. Department of Surgery, Division of Plastic and Reconstructive Surgery, Stanford University School of Medicine, Stanford, United States

5. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States

6. Novartis Institute for Biomedical Research, Cambridge, United States

7. Howard Hughes Medical Institute, Stanford University, Stanford, United States

Abstract

The Xist lncRNA mediates X chromosome inactivation (XCI). Here we show that Spen, an Xist-binding repressor protein essential for XCI , binds to ancient retroviral RNA, performing a surveillance role to recruit chromatin silencing machinery to these parasitic loci. Spen loss activates a subset of endogenous retroviral (ERV) elements in mouse embryonic stem cells, with gain of chromatin accessibility, active histone modifications, and ERV RNA transcription. Spen binds directly to ERV RNAs that show structural similarity to the A-repeat of Xist, a region critical for Xist-mediated gene silencing. ERV RNA and Xist A-repeat bind the RRM domains of Spen in a competitive manner. Insertion of an ERV into an A-repeat deficient Xist rescues binding of Xist RNA to Spen and results in strictly local gene silencing in cis. These results suggest that Xist may coopt transposable element RNA-protein interactions to repurpose powerful antiviral chromatin silencing machinery for sex chromosome dosage compensation.

Funder

National Human Genome Research Institute

Scleroderma Research Foundation

Howard Hughes Medical Institute

National Institute of General Medical Sciences

National Institute of Dental and Craniofacial Research

Hagey Laboratory for Pediatric Regenerative Medicine

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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