Multiple nuclear localization sequences in SRSF4 protein

被引:5
|
作者
Masaki, So [1 ,2 ]
Kabuto, Takafumi [3 ]
Suzuki, Kenji [2 ]
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
关键词
classical-type NLS; NLS; RS domain; SR repeat; SRSF4; SR SPLICING FACTORS; MESSENGER-RNA; RS DOMAIN; FAMILY; PHOSPHORYLATION; IMPORT; DEPHOSPHORYLATION; KINASE; TRANSPORTIN-SR2; REGULATORS;
D O I
10.1111/gtc.12756
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:327 / 333
页数:7
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