Limited expression of nuclear pore membrane glycoprotein 210 in cell lines and tissues suggests cell-type specific nuclear pores in metazoans

被引:70
作者
Olsson, M [1 ]
Schéele, S [1 ]
Ekblom, P [1 ]
机构
[1] Lund Univ, Dept Cell & Mol Biol, Sect Cell & Dev Biol, SE-22184 Lund, Sweden
关键词
nuclear pore membrane; epithelial cell polarity; stem cells;
D O I
10.1016/j.yexcr.2003.09.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The nuclear pore complex (NPC) is the only known gateway for nucleocytoplasmic traffic. The nuclear pore membrane glycoprotein 210 (POM210/gp210) is considered to be important for the assembly and structure of pore complexes in metazoan cells. However, here we demonstrate cell-type specific expression of the gp210 protein during mouse organogenesis. As shown previously for its mRNA, distinct expression of the gp210 was seen in developing epithelia and some other cell types, whereas it was undetectable in nuclei of several other embryonic tissue compartments. In sharp contrast, monoclonal antibody 414 recognizing four non-membrane nucleoporins, stained the nuclear envelope of all cell types. In four cultured mouse cell lines, gp210 mRNA and protein were below detection levels, in contrast to some other nucleoporins tested. Distinct expression of gp210 mRNA and protein was seen in cultured mouse embryonic stem (ES) cells. These findings support the view of cell-type specific NPCs in metazoans and that the gp210 gene is regulated by cell-type specific control elements not shared by other nucleoporins. Although it cannot be excluded that very low expression levels of gp210 are sufficient to allow attachment of NPCs, a more likely alternative is that it has cell-type specific functions. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:359 / 370
页数:12
相关论文
共 38 条
[21]   TRANS-FILTER INDUCTION OF TUBULES IN MOUSE METANEPHROGENIC MESENCHYME [J].
GROBSTEIN, C .
EXPERIMENTAL CELL RESEARCH, 1956, 10 (02) :424-440
[22]   AN INTEGRAL MEMBRANE-PROTEIN OF THE PORE MEMBRANE DOMAIN OF THE NUCLEAR-ENVELOPE CONTAINS A NUCLEOPORIN-LIKE REGION [J].
HALLBERG, E ;
WOZNIAK, RW ;
BLOBEL, G .
JOURNAL OF CELL BIOLOGY, 1993, 122 (03) :513-521
[23]   Removal of a single pore subcomplex results in vertebrate nuclei devoid of nuclear pores [J].
Harel, A ;
Orjalo, AV ;
Vincent, T ;
Lachish-Zalait, A ;
Vasu, S ;
Shah, S ;
Zimmerman, E ;
Elbaum, M ;
Forbes, DJ .
MOLECULAR CELL, 2003, 11 (04) :853-864
[24]   CONTRASTING EXPRESSION PATTERNS OF 3 MEMBERS OF THE MYC FAMILY OF PROTOONCOGENES IN THE DEVELOPING AND ADULT-MOUSE KIDNEY [J].
MUGRAUER, G ;
EKBLOM, P .
JOURNAL OF CELL BIOLOGY, 1991, 112 (01) :13-25
[25]   Transport of proteins and RNAs in and out of the nucleus [J].
Nakielny, S ;
Dreyfuss, G .
CELL, 1999, 99 (07) :677-690
[26]   CDNA cloning and embryonic expression of mouse nuclear pore membrane glycoprotein 210 mRNA [J].
Olsson, M ;
Ekblom, M ;
Fecker, L ;
Kurkinen, M ;
Ekblom, P .
KIDNEY INTERNATIONAL, 1999, 56 (03) :827-838
[27]   Nuclear calcium and the regulation of the nuclear pore complex [J].
PerezTerzic, C ;
Jaconi, M ;
Clapham, DE .
BIOESSAYS, 1997, 19 (09) :787-792
[28]   Polyproline type II conformation in the C-terminal domain of the nuclear pore complex protein gp210 [J].
Pilpel, Y ;
Bogin, O ;
Brumfeld, V ;
Reich, Z .
BIOCHEMISTRY, 2003, 42 (12) :3519-3526
[29]  
POTTER EL, 1965, ARCH PATHOL, V80, P241
[30]   CORRELATION BETWEEN STRUCTURE AND MASS-DISTRIBUTION OF THE NUCLEAR-PORE COMPLEX AND OF DISTINCT PORE COMPLEX COMPONENTS [J].
REICHELT, R ;
HOLZENBURG, A ;
BUHLE, EL ;
JARNIK, M ;
ENGEL, A ;
AEBI, U .
JOURNAL OF CELL BIOLOGY, 1990, 110 (04) :883-894