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The MLLT3 YEATS domain is a dual reader of histone marks (H3K9/18/27ac/cr) and ncRNA (7SK), linking epigenetic and RNA signaling to regulate hematopoiesis.

作者信息

Boulton Adam, Kabra Ashish, Achille Nicholas, Adelman Emmalee R, Anastasakis Dimitrios G, Beckedorff Felipe, Cingaram Pradeepkumar, Zhang Ying, Leach Benjamin, Shiekhattar Ramin, Yokoyama Akihiko, Hafner Markus, Figueroa Maria, Zeleznik-Le Nancy, Bushweller John

机构信息

Dept. of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22903, United States.

Dept. of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44106, United States.

出版信息

bioRxiv. 2025 Sep 3:2025.09.01.673558. doi: 10.1101/2025.09.01.673558.

Abstract

The protein MLLT3 (AF9) is a critical regulator of hematopoiesis. The N-terminal YEATS domain of MLLT3 is an epigenetic reader that binds to acetylated as well as crotonylated lysine. Using PAR-CLIP, biochemical assays, and NMR based mapping of binding, we demonstrate that the YEATS domain of MLLT3 binds to a specific stem-loop region of the noncoding RNA 7SK. 7SK is a noncoding RNA with a well-documented function in transcriptional elongation. We developed point mutations in the YEATS domain that disrupt RNA binding while having no effect on binding of acetylated histone peptides to probe the specific role of RNA binding in MLLT3 function. Our results show loss of RNA binding by MLLT3 skews hematopoietic differentiation away from the myeloid lineage and toward the lymphoid lineage and has substantial effects on gene expression, confirming the essential nature of MLLT3-RNA binding for function.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff6e/12424957/a82c94860a95/nihpp-2025.09.01.673558v1-f0001.jpg

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本文引用的文献

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