A new spectrin, βIV, has a major truncated isoform that associates with promyelocytic leukemia protein nuclear bodies and the nuclear matrix

被引:48
作者
Tse, WT
Tang, J
Jin, O
Korsgren, C
John, KM
Kung, AL
Gwynn, B
Peters, LL
Lux, SE
机构
[1] Childrens Hosp, Div Hematol Oncol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Jackson Lab, Bar Harbor, ME 04609 USA
关键词
D O I
10.1074/jbc.M009307200
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
We isolated cDNAs that encode a 77-kDa peptide similar to repeats 10-16 of beta -spectrins, Its gene localizes to human chromosome 19q13.13-q13.2 and mouse chromosome 7, at 7.5 centimorgans, A 289-kDa isoform, similar to full-length beta -spectrins, was partially assembled from sequences in the human genomic DNA data base and completely cloned and sequenced. RNA transcripts are seen predominantly in the brain, and Western analysis shows a major peptide that migrates as a 72-kDa band. This new gene, spectrin beta IV, thus encodes a full-length minor isoform (Sp beta IV Sigma1) and a truncated major isoform (Sp beta IV Sigma5), Immunostaining of cells shows a micropunctate pattern in the cytoplasm and nucleus. In mesenchymal stem cells, the staining concentrates at nuclear dots that stain positively for the promyelocytic leukemia protein (PML). Expression of Sp beta IV Sigma5 fused to green fluorescence protein in cells produces nuclear dots that include all PML bodies, which double in number in transfected cells. Deletion analysis shows that partial repeats 10 and 16 of Sp beta IV Sigma5 are necessary for nuclear dot formation. Immunostaining of whole-mount nuclear matrices reveals diffuse positivity with accentuation at PML bodies, Spectrin beta IV is the first beta -spectrin associated with a subnuclear structure and may be part of a nuclear scaffold to which gene regulatory machinery binds.
引用
收藏
页码:23974 / 23985
页数:12
相关论文
共 92 条
[1]   The promyelocytic leukemia gene product (PML) forms stable complexes with the retinoblastoma protein [J].
Alcalay, M ;
Tomassoni, L ;
Colombo, E ;
Stoldt, S ;
Grignani, F ;
Fagioli, M ;
Szekely, L ;
Helin, K ;
Pelicci, PG .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (02) :1084-1093
[2]   THE EXON-INTRON ORGANIZATION OF THE HUMAN ERYTHROID BETA-SPECTRIN GENE [J].
AMIN, KM ;
SCARPA, AL ;
WINKELMANN, JC ;
CURTIS, PJ ;
FORGET, BG .
GENOMICS, 1993, 18 (01) :118-125
[3]  
BACHS O, 1990, J BIOL CHEM, V265, P18595
[4]   GOLGI SPECTRIN - IDENTIFICATION OF AN ERYTHROID BETA-SPECTRIN HOMOLOG ASSOCIATED WITH THE GOLGI-COMPLEX [J].
BECK, KA ;
BUCHANAN, JA ;
MALHOTRA, V ;
NELSON, WJ .
JOURNAL OF CELL BIOLOGY, 1994, 127 (03) :707-723
[5]   NUCLEAR PROTEIN MATRIX - ASSOCIATION WITH NEWLY SYNTHESIZED DNA [J].
BEREZNEY, R ;
COFFEY, DS .
SCIENCE, 1975, 189 (4199) :291-293
[6]   IDENTIFICATION OF A NUCLEAR PROTEIN MATRIX [J].
BEREZNEY, R ;
COFFEY, DS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1974, 60 (04) :1410-1417
[7]   βIV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the central and peripheral nervous system [J].
Berghs, S ;
Aggujaro, D ;
Dirkx, R ;
Maksimova, E ;
Stabach, P ;
Hermel, JM ;
Zhang, JP ;
Philbrick, W ;
Slepnev, V ;
Ort, T ;
Solimena, M .
JOURNAL OF CELL BIOLOGY, 2000, 151 (05) :985-1001
[8]   ASSOCIATION OF NUCLEAR MATRIX ANTIGENS WITH EXON-CONTAINING SPLICING COMPLEXES [J].
BLENCOWE, BJ ;
NICKERSON, JA ;
ISSNER, R ;
PENMAN, S ;
SHARP, PA .
JOURNAL OF CELL BIOLOGY, 1994, 127 (03) :593-607
[9]  
Boddy MN, 1996, ONCOGENE, V13, P971
[10]   A deficiency in a 230 kDa DNA repair protein in Fanconi anemia complementation group A cells is corrected by the FANCA cDNA [J].
Brois, DW ;
McMahon, LW ;
Ramos, NI ;
Anglin, LM ;
Walsh, CE ;
Lambert, MW .
CARCINOGENESIS, 1999, 20 (09) :1845-1853