The chromosome peripheral protein nucleolin locates in the chromosome periphery
and functions in chromosome congression
A layer around chromosomes during mitosis was first
observed by light microscopy about 80 years ago, and subsequent electron
microscopic studies revealed a layer of closely packed fibrils and dense
granules around each chromosome. This layer, designated the 'chromosom
periphery', appears at prometaphase and disappears at telophase during
mitosis.
Nucleolin is one of the proteins identified in our proteome analysis of purified human metaphase chromosomes as a chromosome peripheral protein. Nucleolin is known as a multifunctional protein, however, no previous study has demonstrated its functions during mitosis.
Recently, Ma N. et al. (Journal of Cell Science, 120, 2091-2105, 2007) demonstrate that the localization
pattern of nucleolin throughout the cell cycle. Six cells in clockwise
of the cover showed HeLa cells immunostained with antibodies against nucleolin
in green and stained with DAPI in blue. At interphase (top), nucleolin
is prominently localized at the outer layer of the nucleoli, and present
at a lower concentration throughout the nucleoplasm. At prophase (upper
right), most of the nucleolin remains in the nucleolar remnants. When the
nuclear membrane and nucleoli are disrupted at prometaphase (lower right),
nucleolin begins to disperse throughout the cytoplasm and localize at the
chromosome periphery. At metaphase (bottom), nucleolin is localized at
the chromosome periphery and slightly distribute in the cytoplasm. At anaphase
(lower left), most of the nucleolin remains associated with the chromosome
periphery, while some becomes packagcd into cytoplasmic particles known
as nucleolus-derived foci (NDFs). At telophase (upper right), nucleolin
is still associated with chromosomes, and most of it accumulates into NDFs
and pre-nucleolar bodies Nucleolin depletion by RNAi mainly induced two
types of pronounced defects in chromosome congression: misalignment (upper
in the center of the cover) and non-alignment (lower). Two images are nucleolin-depleted
cells immunostained with an antibody against ƒ¿-tubulin in green. a kinetochore marker CREST in red and stained with DAPI
in blue. We show that this defect is due to improper kinetochore attachments,
resulting in reduced tension, and syntelic attachments of microtubules
at the kinetochore.
(Ma Nam, Sachihiro Matsunaga, Hideaki Takata, Uchiyama
Susumu and Kiichi Fukui, Department of Biotechnology, Graduate School of
Engineering, Osaka University, 2-1 Yamadaoka, Suita 565-0871, Osaka, Japan) |