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In\u00a0Saccharomyces cerevisiae, this modification is catalyzed by Set2, an ortholog of the mammalian H3K36 methyltransferase SETD2. Previous genetic, biochemical, and structural studies showed that Set2 activity is repressed by a Set2 autoinhibitory domain (AID) and that activation requires the direct binding of the histone chaperone Spt6. To study the role of Spt6 and Set2 autoinhibition in vivo, we have isolated and analyzed multiple classes of Spt6 and Set2 mutants. Our results suggest an autoinhibited form of Set2 in which the catalytic domain (CD) is bound by the AID. In strong agreement with our genetic results, biophysical experiments demonstrate that the CD and AID physically interact, and that the autoinhibition mutants disrupt this interaction. Finally, RNA sequencing and chromatin immunoprecipitation and sequencing studies show the importance of the Set2\u2013Spt6 interaction for transcription and H3K36 methylation genome-wide. Taken together, our results support a model in which Set2 exists in an inactive, autoinhibited state\u00a0in vivo through direct CD\u2013AID interactions, with binding by Spt6 required to release the autoinhibition.<\/jats:p>","DOI":"10.1093\/nar\/gkag839","type":"journal-article","created":{"date-parts":[[2026,8,14]],"date-time":"2026-08-14T11:19:50Z","timestamp":1786706390000},"source":"Crossref","is-referenced-by-count":0,"title":["Regulation of the histone H3K36 methyltransferase Set2 by the histone chaperone Spt6"],"prefix":"10.1093","volume":"54","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7669-5468","authenticated-orcid":false,"given":"Alexandra R","family":"Elchert","sequence":"first","affiliation":[{"name":"Department of Genetics, Blavatnik Institute, Harvard Medical School , Boston, MA 02115 ,","place":["United 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