ACD15, ACD21, and SLN regulate the accumulation and mobility of MBD6 to silence genes and transposable elements

Author:

Boone Brandon A.12ORCID,Ichino Lucia12ORCID,Wang Shuya12ORCID,Gardiner Jason2ORCID,Yun Jaewon2,Jami-Alahmadi Yasaman3ORCID,Sha Jihui3ORCID,Mendoza Cristy P.2,Steelman Bailey J.2ORCID,van Aardenne Aliya2ORCID,Kira-Lucas Sophia2,Trentchev Isabelle2ORCID,Wohlschlegel James A.3ORCID,Jacobsen Steven E.12345ORCID

Affiliation:

1. Molecular Biology Institute, University of California Los Angeles, Los Angeles, CA 90095, USA.

2. Department of Molecular, Cell and Developmental Biology, University of California Los Angeles, Los Angeles, CA 90095, USA.

3. Department of Biological Chemistry, University of California Los Angeles, Los Angeles, CA 90095, USA.

4. Eli and Edyth Broad Center of Regenerative Medicine and Stem Cell Research, University of California Los Angeles, Los Angeles, CA 90095, USA.

5. Howard Hughes Medical Institute (HHMI), University of California Los Angeles, Los Angeles, CA 90095, USA.

Abstract

DNA methylation mediates silencing of transposable elements and genes in part via recruitment of the Arabidopsis MBD5/6 complex, which contains the methyl-CpG binding domain (MBD) proteins MBD5 and MBD6, and the J-domain containing protein SILENZIO (SLN). Here, we characterize two additional complex members: α-crystalline domain (ACD) containing proteins ACD15 and ACD21. We show that they are necessary for gene silencing, bridge SLN to the complex, and promote higher-order multimerization of MBD5/6 complexes within heterochromatin. These complexes are also highly dynamic, with the mobility of MBD5/6 complexes regulated by the activity of SLN. Using a dCas9 system, we demonstrate that tethering the ACDs to an ectopic site outside of heterochromatin can drive a massive accumulation of MBD5/6 complexes into large nuclear bodies. These results demonstrate that ACD15 and ACD21 are critical components of the gene-silencing MBD5/6 complex and act to drive the formation of higher-order, dynamic assemblies at CG methylation (meCG) sites.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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