H1.X with different properties from other linker histones is required for mitotic progression

FEBS Letters

Volumn 581, Issue 20, 2007, Pages 3783-3788

  Takata, Hideaki ^a   Matsunaga, Sachihiro ^a   Morimoto, Akihiro ^a   Ono Maniwa, Rika ^a   Uchiyama, Susumu ^a   Fukui, Kiichi ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

Chromosome; FRAP; Histone H1; Histone H1.X; Mitosis; RNAi

Indexed keywords

HISTONE H1; PROTEIN SUBUNIT; SMALL INTERFERING RNA;

ACCURACY; ARTICLE; BLEACHING; CHROMATIN; CHROMOSOME; CONTROLLED STUDY; HUMAN; HUMAN CELL; IMMUNOFLUORESCENCE MICROSCOPY; INTERPHASE; MITOSIS; NUCLEOLUS; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DEPLETION; PROTEIN LOCALIZATION; RNA INTERFERENCE; SPINDLE CELL;

CELL NUCLEOLUS; CELL NUCLEUS; CHROMATIN; CHROMOSOMES, HUMAN; FLUORESCENCE RECOVERY AFTER PHOTOBLEACHING; FLUORESCENT ANTIBODY TECHNIQUE, DIRECT; GREEN FLUORESCENT PROTEINS; HELA CELLS; HISTONES; HUMANS; KINETICS; MITOSIS; RNA INTERFERENCE; RNA, SMALL INTERFERING; TRANSFECTION;

EID: 34547106299     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.febslet.2007.06.076     Document Type: Article

References (22)

1. van Holde K.E. Chromatin (1989), Springer-Verlag, New York, NY
2. Shen X., Yu L., Weir J.W., and Gorovsky M.A. Linker histones are not essential and affect chromatin condensation in vivo. Cell 82 (1995) 47-56
3. Maresca T.J., Freedman B.S., and Heald R. Histone H1 is essential for mitotic chromosome architecture and segregation in Xenopus laevis egg extracts. J. Cell Biol. 169 (2005) 859-869
4. Fan Y., Nikitina T., Morin-Kensicki E.M., Zhao J., Magnuson T.R., Woodcock C.L., and Skoultchi A.I. H1 linker histones are essential for mouse development and affect nucleosome spacing in vivo. Mol. Cell Biol. 23 (2003) 4559-4572
5. Rasheed B.K., Whisenant E.C., Ghai R.D., Papaioannou V.E., and Bhatnagar Y.M. Biochemical and immunocytochemical analysis of a histone H1 variant from the mouse testis. J. Cell Sci. 94 (1989) 61-71
6. Parseghian M.H., Henschen A.H., Krieglstein K.G., and Hamkalo B.A. A proposal for a coherent mammalian histone H1 nomenclature correlated with amino acid sequences. Protein Sci. 3 (1994) 575-587
7. Khochbin S., and Wolffe A.P. Developmentally regulated expression of linker-histone variants in vertebrates. Eur. J. Biochem. 225 (1994) 501-510
8. Seyedin S.M., Cole R.D., and Kistler W.S. H1 histones from mammalian testes. The widespread occurrence of H1t. Exp. Cell Res. 136 (1981) 399-405
9. Tanaka M., Hennebold J.D., Macfarlane J., and Adashi E.Y. A mammalian oocyte-specific linker histone gene H1oo: homology with the genes for the oocyte-specific cleavage stage histone (cs-H1) of sea urchin and the B4/H1M histone of the frog. Development 128 (2001) 655-664
10. Yan W., Ma L., Burns K.H., and Matzuk M.M. HILS1 is a spermatid-specific linker histone H1-like protein implicated in chromatin remodeling during mammalian spermiogenesis. Proc. Natl. Acad. Sci. USA 100 (2003) 10546-10551
11. Yamamoto T., and Horikoshi M. Cloning of the cDNA encoding a novel subtype of histone H1. Gene 173 (1996) 281-285
12. Uchiyama S., Kobayashi S., Takata H., Ishihara T., Hori N., Higashi T., Hayashihara K., Sone T., Higo D., Nirasawa T., Takao T., Matsunaga S., and Fukui K. Proteome analysis of human metaphase chromosomes. J. Biol. Chem. 280 (2005) 16994-17004
13. Takata H., Uchiyama S., Nakamura N., Nakashima S., Kobayashi S., Sone T., Kimura S., Lahmers S., Granzier H., Labeit S., Matsunaga S., and Fukui K. A comparative proteome analysis of human metaphase chromosomes isolated from two different cell lines reveals a set of conserved chromosome-associated proteins. Genes Cells 12 (2007) 269-284
14. Cole R.D. Microheterogeneity in H1 histones and its consequences. Int. J. Pept. Protein Res. 30 (1987) 433-449
15. Happel N., Schulze E., and Doenecke D. Characterisation of human histone H1x. Biol. Chem. 386 (2005) 541-551
16. Chen D., Dundr M., Wang C., Leung A., Lamond A., Misteli T., and Huang S. Condensed mitotic chromatin is accessible to transcription factors and chromatin structural proteins. J. Cell Biol. 168 (2005) 41-54
17. Misteli T., Gunjan A., Hock R., Bustin M., and Brown D.T. Dynamic binding of histone H1 to chromatin in living cells. Nature 408 (2000) 877-881
18. Hendzel M.J., Lever M.A., Crawford E., and Th'ng J.P. The C-terminal domain is the primary determinant of histone H1 binding to chromatin in vivo. J. Biol. Chem. 279 (2004) 20028-20034
19. Brown D.T., Izard T., and Misteli T. Mapping the interaction surface of linker histone H1(0) with the nucleosome of native chromatin in vivo. Nat. Struct. Mol. Biol. 13 (2006) 250-255
20. Ponte I., Vidal-Taboada J.M., and Suau P. Evolution of the vertebrate H1 histone class: evidence for the functional differentiation of the subtypes. Mol. Biol. Evol. 15 (1998) 702-708
21. van Hooser A.A., Yuh P., and Heald R. The perichromosomal layer. Chromosoma 114 (2005) 377-388
22. Ma N., Matsunaga S., Takata H., Ono-Maniwa R., Uchiyama S., and Fukui K. Nucleolin functions in nucleolus formation and chromosome congression. J. Cell Sci. 120 (2007) 2091-2105