Emp is a component of the nuclear matrix of mammalian cells and undergoes dynamic rearrangements during cell division

被引:18
作者
Bala, S [1 ]
Kumar, A [1 ]
Soni, S [1 ]
Sinha, S [1 ]
Hanspal, M [1 ]
机构
[1] Tufts Univ, Sch Med, Caritas St Elizabeths Med Ctr, Ctr Cell Biol,Dept Med, Boston, MA 02135 USA
关键词
Emp; nuclear matrix; actin; erythroblast; macrophage; nuclear actin; mitosis; cytokinesis;
D O I
10.1016/j.bbrc.2006.02.060
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
Emp, originally detected in erythroblastic islands, is expressed in numerous cell types and tissues suggesting a functionality not limited to hematopoiesis. To study the function of Emp in non-hematopoietic cells, an epitope-tagged recombinant human Emp was expressed in HEK cells. Preliminary studies revealed that Emp partitioned into both the nuclear and Triton X-100-insoluble cytoskeletal fractions in approximately a 4:1 ratio. In this study, we report investigations of Emp in the nucleus. Sequential extractions of interphase nuclei showed that recombinant Emp was present predominantly in the nuclear matrix. Immunofluorescence microscopy showed that Emp was present in typical nuclear speckles enriched with the spliceosome assembly factor SC35 and partially co-localized with actin staining. Coimmunoprecipitation and GST-pull-down assays confirmed the apparent close association of Emp with nuclear actin. During mitosis, Emp was detected at the mitotic spindle/spindle poles, as well as in the contractile ring during cytokinesis. These results suggest that Emp undergoes dynamic rearrangements within the nuclear architecture that are correlated with cell division. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1040 / 1048
页数:9
相关论文
共 50 条
[1]   NUCLEAR PROTEIN MATRIX - ASSOCIATION WITH NEWLY SYNTHESIZED DNA [J].
BEREZNEY, R ;
COFFEY, DS .
SCIENCE, 1975, 189 (4199) :291-293
[2]   INSITU LOCALIZATION OF DNA TOPOISOMERASE-II, A MAJOR POLYPEPTIDE COMPONENT OF THE DROSOPHILA NUCLEAR MATRIX-FRACTION [J].
BERRIOS, M ;
OSHEROFF, N ;
FISHER, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (12) :4142-4146
[3]   NUCLEAR ELIMINATION FROM NORMOBLAST OF FETAL GUINEA PIG LIVER AS STUDIED WITH ELECTRON MICROSCOPY AND SERIAL SECTIONING TECHNIQUES [J].
CAMPBELL, FR .
ANATOMICAL RECORD, 1968, 160 (03) :539-+
[4]   THE NUCLEAR MATRIX - 3-DIMENSIONAL ARCHITECTURE AND PROTEIN-COMPOSITION [J].
CAPCO, DG ;
WAN, KM ;
PENMAN, S .
CELL, 1982, 29 (03) :847-858
[5]   SEQUENCE REQUIREMENTS FOR SYNTHETIC PEPTIDE-MEDIATED TRANSLOCATION TO THE NUCLEUS [J].
CHELSKY, D ;
RALPH, R ;
JONAK, G .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (06) :2487-2492
[6]  
CIEJEK EM, 1983, NATURE, V306, P607, DOI 10.1038/306607a0
[7]   DIFFUSIBLE AND BOUND ACTIN IN NUCLEI OF XENOPUS-LAEVIS OOCYTES [J].
CLARK, TG ;
MERRIAM, RW .
CELL, 1977, 12 (04) :883-891
[8]   CDNA SEQUENCING OF NUCLEAR LAMIN-A AND LAMIN-C REVEALS PRIMARY AND SECONDARY STRUCTURAL HOMOLOGY TO INTERMEDIATE FILAMENT PROTEINS [J].
FISHER, DZ ;
CHAUDHARY, N ;
BLOBEL, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (17) :6450-6454
[9]   SOLUBILIZATION AND PURIFICATION OF ENZYMATICALLY ACTIVE GLUTATHIONE-S-TRANSFERASE (PGEX) FUSION PROTEINS [J].
FRANGIONI, JV ;
NEEL, BG .
ANALYTICAL BIOCHEMISTRY, 1993, 210 (01) :179-187
[10]   FACTOR REQUIRED FOR MAMMALIAN SPLICEOSOME ASSEMBLY IS LOCALIZED TO DISCRETE REGIONS IN THE NUCLEUS [J].
FU, XD ;
MANIATIS, T .
NATURE, 1990, 343 (6257) :437-441