Identification and characterization of a novel cytoplasm protein ICF45 that is involved in cell cycle regulation

被引:22
作者
Guo, DL
Hu, K
Lei, Y
Wang, YC
Ma, TL
He, DC [1 ]
机构
[1] Beijing Normal Univ, Coll Life Sci, Minist Educ, Key Lab Cell Proliferat & Regulat Biol, Beijing 100875, Peoples R China
[2] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
关键词
D O I
10.1074/jbc.M406737200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A novel cytoplasm protein, interphase cytoplasm foci protein 45 kDa (ICF45), was identified by screening the cDNA expression library for HeLa cells with serum from an autoimmune patient. The complete cDNA sequence of ICF45 was determined to be 1.32 kb and to encode 298 amino acids with an apparent molecular mass of 45 kDa. The ICF45 transcripts were detected in different tissues and were relatively rich in human liver and lung tissues but scarce in brain tissue. Immunofluorescence with anti-ICF45-specific antibodies demonstrated that ICF45 is strongly expressed in interphase and cannot be seen in mitosis. The subcellular localization of ICF45 and fusion proteins GFP-ICF45, ICF45-GFP, and HA-ICF45 showed ICF45 centralized into 1 - 2 dots in the cytoplasm and always near the nuclear membrane. The staining foci of ICF45 appeared to be slightly larger than centrosomes and in some cases were found to colocalize with centrosomes. After effectively silencing the ICF45 by RNAi, the growth and proliferation of the cells were significantly inhibited, and p53 was detected to be up-regulated. The silencing of ICF45 also resulted in an appearance of polycentrosome and multinuclear cells, which finally went to apoptosis. Our results suggest that ICF45 is a highly conserved novel protein, which is expressed in a cell cycle-dependent manner and seemed to be involved in cell cycle progression and cell proliferation.
引用
收藏
页码:53498 / 53505
页数:8
相关论文
共 26 条
[1]   HUMAN AUTOANTIBODY TO A NOVEL PROTEIN OF THE NUCLEAR COILED BODY - IMMUNOLOGICAL CHARACTERIZATION AND CDNA CLONING OF P80-COILIN [J].
ANDRADE, LEC ;
CHAN, EKL ;
RASKA, I ;
PEEBLES, CL ;
ROOS, G ;
TAN, EM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (06) :1407-1419
[2]  
Brinkley BR, 1998, CELL MOTIL CYTOSKEL, V41, P281, DOI 10.1002/(SICI)1097-0169(1998)41:4<281::AID-CM1>3.0.CO
[3]  
2-C
[4]  
CHAN EKL, 1992, RHEUM DIS CLIN N AM, V18, P551
[5]   Mammalian centromeres: DNA sequence, protein composition, and role in cell cycle progression [J].
Craig, JM ;
Earnshaw, WC ;
Vagnarelli, P .
EXPERIMENTAL CELL RESEARCH, 1999, 246 (02) :249-262
[6]   CDNA CLONING OF HUMAN DNA TOPOISOMERASE-I - CATALYTIC ACTIVITY OF A 67.7-KDA CARBOXYL-TERMINAL FRAGMENT [J].
DARPA, P ;
MACHLIN, PS ;
RATRIE, H ;
ROTHFIELD, NF ;
CLEVELAND, DW ;
EARNSHAW, WC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (08) :2543-2547
[7]   Human antibodies in cancer and autoimmune disease [J].
Ditzel, HJ .
IMMUNOLOGIC RESEARCH, 2000, 21 (2-3) :185-193
[8]   IDENTIFICATION OF A FAMILY OF HUMAN CENTROMERE PROTEINS USING AUTOIMMUNE SERA FROM PATIENTS WITH SCLERODERMA [J].
EARNSHAW, WC ;
ROTHFIELD, N .
CHROMOSOMA, 1985, 91 (3-4) :313-321
[9]   Predicting subcellular localization of proteins based on their N-terminal amino acid sequence [J].
Emanuelsson, O ;
Nielsen, H ;
Brunak, S ;
von Heijne, G .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 300 (04) :1005-1016
[10]   The PROSITE database, its status in 2002 [J].
Falquet, L ;
Pagni, M ;
Bucher, P ;
Hulo, N ;
Sigrist, CJA ;
Hofmann, K ;
Bairoch, A .
NUCLEIC ACIDS RESEARCH, 2002, 30 (01) :235-238