Analysis of the subcellular localization of the human histone methyltransferase SETDB1

SET domain, bifurcated 1 (SETDB1) is a histone methyltransferase that methylates lysine 9 on histone H3. Although it is important to know the localization of proteins to elucidate their physiological function, little is known of the subcellular localization of human SETDB1. In the present study, to...

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Veröffentlicht in:Biochemical and biophysical research communications 2015-10, Vol.465 (4), p.725-731
Hauptverfasser: Tachibana, Keisuke, Gotoh, Eiko, Kawamata, Natsuko, Ishimoto, Kenji, Uchihara, Yoshie, Iwanari, Hiroko, Sugiyama, Akira, Kawamura, Takeshi, Mochizuki, Yasuhiro, Tanaka, Toshiya, Sakai, Juro, Hamakubo, Takao, Kodama, Tatsuhiko, Doi, Takefumi
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Sprache:eng
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Zusammenfassung:SET domain, bifurcated 1 (SETDB1) is a histone methyltransferase that methylates lysine 9 on histone H3. Although it is important to know the localization of proteins to elucidate their physiological function, little is known of the subcellular localization of human SETDB1. In the present study, to investigate the subcellular localization of hSETDB1, we established a human cell line constitutively expressing enhanced green fluorescent protein fused to hSETDB1. We then generated a monoclonal antibody against the hSETDB1 protein. Expression of both exogenous and endogenous hSETDB1 was observed mainly in the cytoplasm of various human cell lines. Combined treatment with the nuclear export inhibitor leptomycin B and the proteasome inhibitor MG132 led to the accumulation of hSETDB1 in the nucleus. These findings suggest that hSETDB1, localized in the nucleus, might undergo degradation by the proteasome and be exported to the cytosol, resulting in its detection mainly in the cytosol. •Endogenous human SETDB1 was localized mainly in the cytoplasm.•Combined treatment with LMB and MG132 led to accumulation of human SETDB1 in the nucleus.•HeLa cells expressing EFGP-hSETDB1 are useful for subcellular localization analyses.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2015.08.065