Comprehensive analysis of the ICEN (Interphase Centromere Complex) components enriched in the CENP‐A chromatin of human cells

The centromere is a chromatin structure essential for correct segregation of sister chromatids, and defects in this region often lead to aneuploidy and cancer. We have previously reported purification of the interphase centromere complex (ICEN) from HeLa cells, and have demonstrated the presence of 40 proteins (ICEN1–40), along with CENP‐A, ‐B, ‐C, ‐H and hMis6, by proteomic analysis. Here we report analysis of seven ICEN components with unknown function. Centromere localization of EGFP‐tagged ICEN22, 24, 32, 33, 36, 37 and 39 was observed in transformant cells. Depletion of each of these proteins by short RNA interference produced abnormal metaphase cells carrying misaligned chromosomes and also produced cells containing aneuploid chromosomes, implying that these ICEN proteins take part in kinetochore functions. Interestingly, in the ICEN22, 32, 33, 37 or 39 siRNA‐transfected cells, CENP‐H and hMis6 signals disappeared from all the centromeres in abnormal mitotic cells containing misaligned chromosomes. These results suggest that the seven components of the ICEN complex are predominantly localized at the centromeres and are required for kinetochore function perhaps through or not through loading of CENP‐H and hMis6 onto the centromere.

[1]  H. Kimura,et al.  The Constitutive Centromere Component CENP-50 Is Required for Recovery from Spindle Damage , 2005, Molecular and Cellular Biology.

[2]  S. Grewal,et al.  Ubiquitin ligase component Cul4 associates with Clr4 histone methyltransferase to assemble heterochromatin , 2005, Nature Cell Biology.

[3]  T. Tomonaga,et al.  Centromere protein H is up-regulated in primary human colorectal cancer and its overexpression induces aneuploidy. , 2005, Cancer research.

[4]  S. Narumiya,et al.  Ect2 and MgcRacGAP regulate the activation and function of Cdc42 in mitosis , 2005, The Journal of cell biology.

[5]  Osamu Iwasaki,et al.  A conserved Mis12 centromere complex is linked to heterochromatic HP1 and outer kinetochore protein Zwint-1 , 2004, Nature Cell Biology.

[6]  Karolin Luger,et al.  Structural determinants for generating centromeric chromatin , 2004, Nature.

[7]  Geert J P L Kops,et al.  Lethality to human cancer cells through massive chromosome loss by inhibition of the mitotic checkpoint. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Xiaoping Du,et al.  cDNA cloning and characterization of a novel gene encoding the MLF1-interacting protein MLF1IP , 2004, Oncogene.

[9]  S. Narumiya,et al.  Cdc42 and mDia3 regulate microtubule attachment to kinetochores , 2004, Nature.

[10]  C. Obuse,et al.  Proteomics analysis of the centromere complex from HeLa interphase cells: UV‐damaged DNA binding protein 1 (DDB‐1) is a component of the CEN‐complex, while BMI‐1 is transiently co‐localized with the centromeric region in interphase , 2004, Genes to cells : devoted to molecular & cellular mechanisms.

[11]  D. Reinberg,et al.  Functional Analysis of the Subunits of the Chromatin Assembly Factor RSF , 2003, Molecular and Cellular Biology.

[12]  Shou-Jiang Gao,et al.  Identification of a Novel Cellular Transcriptional Repressor Interacting with the Latent Nuclear Antigen of Kaposi's Sarcoma-Associated Herpesvirus , 2003, Journal of Virology.

[13]  G. Orphanides,et al.  FACT Facilitates Transcription-Dependent Nucleosome Alteration , 2003, Science.

[14]  L. Hennighausen,et al.  Identification of genes differentially expressed in mouse mammary epithelium transformed by an activated β-catenin , 2003, Oncogene.

[15]  K. Yoda,et al.  Human CENP-I specifies localization of CENP-F, MAD1 and MAD2 to kinetochores and is essential for mitosis , 2003, Nature Cell Biology.

[16]  K. Sullivan,et al.  Centromeres and Kinetochores From Epigenetics to Mitotic Checkpoint Signaling , 2003, Cell.

[17]  G. Goshima,et al.  Human centromere chromatin protein hMis12, essential for equal segregation, is independent of CENP-A loading pathway , 2003, The Journal of cell biology.

[18]  H. Masumoto,et al.  CENP-B box is required for de novo centromere chromatin assembly on human alphoid DNA , 2002, The Journal of cell biology.

[19]  T. Ikemura,et al.  CENP-I is essential for centromere function in vertebrate cells. , 2002, Developmental cell.

[20]  K. Yoda,et al.  CENP-A, -B, and -C Chromatin Complex That Contains the I-Type α-Satellite Array Constitutes the Prekinetochore in HeLa Cells , 2002, Molecular and Cellular Biology.

[21]  H. Masumoto,et al.  Human CENP-H multimers colocalize with CENP-A and CENP-C at active centromere--kinetochore complexes. , 2000, Human molecular genetics.

[22]  M. Yanagida,et al.  Requirement of Mis6 centromere connector for localizing a CENP-A-like protein in fission yeast. , 2000, Science.

[23]  K. Yoda,et al.  Human centromere protein A (CENP-A) can replace histone H3 in nucleosome reconstitution in vitro. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[24]  S. Henikoff,et al.  Heterochromatic deposition of centromeric histone H3-like proteins. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[25]  S. Henikoff,et al.  Cell division: A histone-H3-like protein in C. elegans , 1999, Nature.

[26]  G. Karpen,et al.  Centromere proteins and chromosome inheritance: a complex affair. , 1999, Current opinion in genetics & development.

[27]  K. Kinzler,et al.  Genetic instabilities in human cancers , 1998, Nature.

[28]  M. Sekiguchi Genes to cells: edited by Jun-ichi Tomizawa, Blackwell Science Ltd. Institutional: £218.00 (Europe), £242.00 (Rest of World), US$382.00 (USA and Canada). Individual: £65.00 (Europe), £72.00 (Rest of World), US$114.00 (USA and Canada) ISSN 1356 9597 , 1997 .

[29]  K. Sullivan,et al.  Assembly of CENP-A into Centromeric Chromatin Requires a Cooperative Array of Nucleosomal DNA Contact Sites , 1997, The Journal of cell biology.

[30]  S. Stoler,et al.  A mutation in CSE4, an essential gene encoding a novel chromatin-associated protein in yeast, causes chromosome nondisjunction and cell cycle arrest at mitosis. , 1995, Genes & development.

[31]  K. Sullivan,et al.  Human CENP-A contains a histone H3 related histone fold domain that is required for targeting to the centromere , 1994, The Journal of cell biology.

[32]  K. Kimura,et al.  Identification of the nature of modification that causes the shift of DNA topoisomerase II beta to apparent higher molecular weight forms in the M phase. , 1994, The Journal of biological chemistry.

[33]  H. Masumoto,et al.  Distribution of CENP-B boxes reflected in CREST centromere antigenic sites on long-range alpha-satellite DNA arrays of human chromosome 21. , 1994, Human molecular genetics.

[34]  N. Nomura,et al.  Complete sequencing and characterization of 21,243 full-length human cDNAs , 2004, Nature Genetics.

[35]  R. Allshire,et al.  Kinetochore and heterochromatin domains of the fission yeast centromere , 2004, Chromosome Research.

[36]  K. Yoda,et al.  Immunological analysis and purification of centromere complex. , 2004, Methods in enzymology.

[37]  K. Mikoshiba,et al.  A variant of yellow fluorescent protein with fast and efficient maturation for cell-biological applications , 2002, Nature Biotechnology.

[38]  Nihon Hassei Seibutsu Gakkai,et al.  Genes to cells , 1996 .