Multiple nuclear localization sequences in SRSF4 protein
被引:5
|
作者:
Masaki, So
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Kyoto Univ, Grad Sch Med, Med Innovat Ctr, Lab Malignancy Control Res, Kyoto, Japan
Ritsumeikan Univ, Dept Pharmaceut Sci, Lab Mol Med Sci, Shiga, JapanKyoto Univ, Grad Sch Med, Med Innovat Ctr, Lab Malignancy Control Res, Kyoto, Japan
Masaki, So
[1
,2
]
Kabuto, Takafumi
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Kyoto Univ, Lab Anat & Dev Biol, Sch Med, Kyoto, JapanKyoto Univ, Grad Sch Med, Med Innovat Ctr, Lab Malignancy Control Res, Kyoto, Japan
Kabuto, Takafumi
[3
]
Suzuki, Kenji
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Ritsumeikan Univ, Dept Pharmaceut Sci, Lab Mol Med Sci, Shiga, JapanKyoto Univ, Grad Sch Med, Med Innovat Ctr, Lab Malignancy Control Res, Kyoto, Japan
Suzuki, Kenji
[2
]
Kataoka, Naoyuki
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Kyoto Univ, Grad Sch Med, Med Innovat Ctr, Lab Malignancy Control Res, Kyoto, Japan
Kyoto Univ, Lab Anat & Dev Biol, Sch Med, Kyoto, Japan
Univ Tokyo, Grad Sch Agr & Life Sci, Dept Anim Resource Sci, Lab Cellular Biochem, Tokyo, JapanKyoto Univ, Grad Sch Med, Med Innovat Ctr, Lab Malignancy Control Res, Kyoto, Japan
Kataoka, Naoyuki
[1
,3
,4
]
机构:
[1] Kyoto Univ, Grad Sch Med, Med Innovat Ctr, Lab Malignancy Control Res, Kyoto, Japan
[2] Ritsumeikan Univ, Dept Pharmaceut Sci, Lab Mol Med Sci, Shiga, Japan
[3] Kyoto Univ, Lab Anat & Dev Biol, Sch Med, Kyoto, Japan
[4] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Anim Resource Sci, Lab Cellular Biochem, Tokyo, Japan
SRSF4 is one of the members of serine-/arginine (SR)-rich protein family involved in both constitutive and alternative splicing. SRSF4 is localized in the nucleus with speckled pattern, but its nuclear localization signal was not determined. Here, we have identified nuclear localization signals (NLSs) of SRSF4 by using a pyruvate kinase fusion system. As expected, arginine-/serine (RS)-rich domain of SRSF4 confers nuclear localization activity when it is fused to PK protein. We then further delineated the minimum sequences for nuclear localization in RS domain of SRSF4. Surprisingly, RS-rich region does not always have a nuclear localization activity. In addition, basic amino acid stretches that resemble to classical-type NLSs were identified. These results strongly suggest that SRSF4 protein uses two different nuclear import pathways with multiple NLSs in RS domain.