TY - JOUR
T1 - Structure-function conservation between the methyltransferases SETD3 and SETD6
AU - Admoni-Elisha, Lee
AU - Abaev-Schneiderman, Elina
AU - Cohn, Ofir
AU - Shapira, Guy
AU - Shomron, Noam
AU - Feldman, Michal
AU - Levy, Dan
N1 - Publisher Copyright:
© 2022 Elsevier B.V. and Société Française de Biochimie et Biologie Moléculaire (SFBBM)
PY - 2022/9
Y1 - 2022/9
N2 - Among the protein lysine methyltransferases family members, it appears that SETD6 is highly similar and closely related to SETD3. The two methyltransferases show high similarity in their structure, which raised the hypothesis that they share cellular functions. Using a proteomic screen, we identified 52 shared interacting-proteins. Gene Ontology (GO) analysis of the shared proteins revealed significant enrichment of proteins involved in transcription. Our RNA-seq data of SETD6 KO and SETD3 KO HeLa cells identified ∼100 up-regulated and down-regulated shared genes. We have also identified a substantial number of genes that changed dramatically in the double KO cells but did not significantly change in the single KO cells. GO analysis of these genes revealed enrichment of apoptotic genes. Accordingly, we show that the double KO cells displayed high apoptotic levels, suggesting that SETD6 and SETD3 inhibit apoptosis. Collectively, our data strongly suggest a functional link between SETD6 and SETD3 in the regulation of apoptosis.
AB - Among the protein lysine methyltransferases family members, it appears that SETD6 is highly similar and closely related to SETD3. The two methyltransferases show high similarity in their structure, which raised the hypothesis that they share cellular functions. Using a proteomic screen, we identified 52 shared interacting-proteins. Gene Ontology (GO) analysis of the shared proteins revealed significant enrichment of proteins involved in transcription. Our RNA-seq data of SETD6 KO and SETD3 KO HeLa cells identified ∼100 up-regulated and down-regulated shared genes. We have also identified a substantial number of genes that changed dramatically in the double KO cells but did not significantly change in the single KO cells. GO analysis of these genes revealed enrichment of apoptotic genes. Accordingly, we show that the double KO cells displayed high apoptotic levels, suggesting that SETD6 and SETD3 inhibit apoptosis. Collectively, our data strongly suggest a functional link between SETD6 and SETD3 in the regulation of apoptosis.
KW - Methyltransferases
KW - SETD3
KW - SETD6
UR - http://www.scopus.com/inward/record.url?scp=85130407696&partnerID=8YFLogxK
U2 - 10.1016/j.biochi.2022.05.003
DO - 10.1016/j.biochi.2022.05.003
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C2 - 35550916
AN - SCOPUS:85130407696
SN - 0300-9084
VL - 200
SP - 27
EP - 35
JO - Biochimie
JF - Biochimie
ER -