Publications
(*) Denotes first co-authorship
(†) Denotes corresponding authorship
26. Monteagudo-Sánchez A.*, Richard Albert J.*, Scarpa M., Noordermeer D., Greenberg M.V.C. (2024) The impact of the embryonic DNA methylation program on CTCF-mediated genome regulation. Nucleic Acids Res. Link
25. Monteagudo-Sánchez A., Noordermeer D., Greenberg M.V.C. (2024) The impact of DNA methylation on CTCF-mediated 3D genome organization. Nat Struct Mol Biol. Link
24. Schulz M., Teissandier A., De La Mata Santaella E., Armand M., Iranzo J., El Marjou F., Gestraud P., Walter M., Kinston S., Göttgens B., Greenberg M.V.C., Bourc'his D. (2024) DNA methylation restricts coordinated germline and neural fates in embryonic stem cell differentiation. Nat Struct Mol Biol. Link
23. Yakhou L., Azogui A., Gupta N., Richard Albert J., Miura F., Ferry L., Yamaguchi K., Battault S., Therizols P., Bonhomme F., Bethuel E., Sarkar A., Greenberg M.V.C., Arimondo P.B., Cristofari G., Kirsh O., Ito T., Defossez P-A. (2023) A genetic screen identifies BEND3 as a regulator of bivalent gene expression and global DNA methylation. Nucleic Acids Res. Link
22. Canat A., Veillet A., Batrin R., Dubourg C., Lhoumaud P., Arnau-Romero P., Greenberg M.V.C., Bonhomme F., Arimondo P.B., Illingworth R., Fabre E., Therizols P. (2023) DAXX safeguards heterochromatin formation in embryonic stem cells. J Cell Sci. Link
21. Gupta N., Yakhou L., Richard Albert J., Azogui A., Ferry L., Kirsh O., Miura F., Battault S., Yamaguchi K., Laisné M., Domrane C., Bonhomme F., Sarkar A., Delagrange M., Ducos B., Cristofari G., Ito T., Greenberg M.V.C., Defossez P-A. (2023) A genome-wide screen reveals new regulators of the 2-cell-like cell state. Nat Struct Mol Biol. Link
20. Richard Albert J., Greenberg M.V.C. ( 2023) Non-canonical imprinting in the spotlight. Development Link
19. Dubois A., Vincenti L., Chervova A. , Greenberg M.V.C., Vandormael-Pournin S., Bourc'his D., Cohen-Tannoudji M., Navarro P. ( 2022) H3K9 tri-methylation at Nanog times differentiation commitment and enables the acquisition of primitive endoderm fate. Development Link
18. Manceau L., Richard Albert J., Lollini P.L., Greenberg M.V.C., Gilardi-Hebenstreit P., Ribes V. (2022) Divergent transcriptional and transforming properties of PAX3-FOXO1 and PAX7-FOXO1 paralogs. PLOS Genetics Link
17. Richard Albert J., Greenberg M.V.C. (2021) The Polycomb landscape in mouse development. Nature Genetics Link
16. Greenberg M.V.C. (2021) Get Out and Stay Out: New Insights Into DNA Methylation Reprogramming in Mammals. Frontiers in Cell and Developmental Biology Link
15. Greenberg M.V.C., Bourc’his D. (2019) The diverse roles of DNA methylation in mammalian development and disease. Nature Reviews Molecular Cell Biology Link
14. Greenberg M.V.C.†, Teissandier A., Walter, M., Noordermeer D., Bourc’his D†. (2019) Dynamic enhancer partitioning instructs activation of a growth-related gene during exit from naïve pluripotency. eLife 8:e44057 Link
13. Greenberg M.V.C.*, Glaser J.*, Borsos M., El Marjou F., Walter M., Teissandier A., Bourc'his D. (2017) Transient transcription in the early embryo sets an epigenetic state that programs postnatal growth. Nature Genetics 49:110-118 Link
12. Greenberg M.V.C., Bourc’his D. (2015) Cultural relativism: maintenance of genomic imprints in pluripotent stem cell culture systems. Curr. Op. Genet. & Dev. 31:42–49. Review Article Link
11. Zhang S., Zhou B., Kang Y., Cui X., Liu A., Deleris A., Greenberg M.V.C., Cui X., Qiu Q., Lu F., Wohlschlegel J.A., Jacobsen S.E., Cao X. (2015) C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association. Cell Discovery 1:15003 Link
10. Groth M., Stroud H., Feng S., Greenberg M.V.C., Vashisht A.A., Wohlschlegel J.A., Jacobsen S.E., Ausin I. (2014) SNF2 chromatin remodeler-family proteins FRG1 and -2 are required for RNA-directed DNA methylation. Proc. Nat. Acad. Sci. U.S.A. 111:17666-17671 Link
9. Duffié R., Ajjan S., Greenberg M.V.C., Zamudio N., Escamilla del Arenal M., Iranzo J., Okamoto I., Barbaux S., Fauque P., Bourc’his D. (2014) The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals. Genes & Dev. 28:463–478 Link
8. Greenberg M.V.C.*, Deleris A.*, Hale C.J.*, Liu A., Feng S., Jacobsen S.E. (2013) Interplay between active chromatin marks and RNA-directed DNA methylation in Arabidopsis thaliana. PLoS Genet. 9(11): e1003946, 1-11 Link
7. Stroud H., Greenberg M.V.C., Feng S., Bernatavichute Y.V., Jacobsen S.E. (2013) Comprehensive analysis of silencing mutants reveals complex regulation of the Arabidopsis methylome. Cell 152: 352-64 Link
6. Caro E., Stroud H., Greenberg M.V.C., Bernatavichute Y.V., Feng S., Groth M., Vashisht A.A., Wohlschlegel J.A., Jacobsen S.E. (2012) The SET-domain protein SUVR5 mediates H3K9me2 deposition and silencing at stimulus response genes in a DNA methylation independent manner. PLoS Genet. 8: e1002995, 1-12 Link
5. Ausin I.*, Greenberg M.V.C.*, Simanshu D.K.*, Hale C.J., Vashisht A.A., Simon S.A., Lee T., Feng S., Espanola S.D., Meyers B.C., Wohlschlegel J.A., Patel D.J., Jacobsen S.E. (2012) INVOLVED IN DE NOVO 2 containing complex involved in RNA-directed DNA methylation in Arabidopsis. Proc. Nat. Acad. Sci. U. S. A. 109: 8374-8381 Link
4. Ausin I.*, Greenberg M.V.C.*, Li C.F., Jacobsen S.E. (2011) The splicing factor SR45 affects the RNA-directed DNA methylation pathway in Arabidopsis. Epigenetics 7:29-33 Link
3. Greenberg M.V.C., Ausin I., Chan S.W.L., Cokus S.J., Cuperus J.T., Feng S., Law J.A., Chu C., Pellegrini M., Carrington J.C., Jacobsen S.E. (2011) Identification of genes required for de novo DNA methylation in Arabidopsis. Epigenetics 6:344-354 Link
2. Deleris A.*, Greenberg M.V.C.*, Ausin I., Law R.W.Y., Moissiard G., Schubert D., Jacobsen S.E. (2010) Involvement of a Jumonji-C domain-containing histone demethylase in DRM2-mediated maintenance of DNA Methylation. EMBO Rep.11: 950-955 Link