HIGH AND LOW-MOLECULAR-WEIGHT TAU-PROTEINS ARE DIFFERENTIALLY EXPRESSED FROM A SINGLE-GENE

被引:29
作者
MAVILIA, C
COUCHIE, D
MATTEI, MG
NIVEZ, MP
NUNEZ, J
机构
[1] HOP HENRI MONDOR,INSERM,U282,F-94010 CRETEIL,FRANCE
[2] HOP ENFANTS LA TIMONE,CTR GENET MED,INSERM,U242,F-13385 MARSEILLE 4,FRANCE
关键词
TAU-PROTEINS; SPINAL CORD; DEVELOPMENT; GENE;
D O I
10.1111/j.1471-4159.1993.tb03622.x
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
Both high and low molecular weight (HMW and LMW) tau proteins are expressed in the immature and adult mouse spinal cord. Northern blot analysis, performed with probes complementary to domains common and uncommon to the LMW and HMW entities, suggested that HMW tau proteins found in the immature mouse spinal cord are not translated from the single transcript of 6 kb expressed at these stages, but are transported within this nervous structure by axons arising in the periphery. In contrast, another minor transcript of 8 kb was detected in the adult mouse spinal cord by a HMW tau Specific probe, suggesting that a small fraction of the HMW tau forms present in adulthood are translated within mouse spinal cord neurons. LMW spinal cord tau forms are encoded by mRNAs of 6 kb that contain three and four homologous repeats at immature and mature stages, respectively, whereas adult HMW entities contain four repeats. PCR analysis performed with mouse genomic DNA also showed that the nonhomologous region specific for HMW tau is a single exon. Southern blot and gene mapping showed that the same gene, located on the murine chromosome 11, encodes all the LMW and HMW tau variants. All these tau forms, therefore, are produced by an alternative splicing mechanism that is neuron-specific and developmentally regulated.
引用
收藏
页码:1073 / 1081
页数:9
相关论文
共 43 条
[21]  
GEORGIEFF IS, 1992, MOL BIOL CELL, V3, pA165
[22]   CLONING OF A BIG TAU-MICROTUBULE-ASSOCIATED PROTEIN CHARACTERISTIC OF THE PERIPHERAL NERVOUS-SYSTEM [J].
GOEDERT, M ;
SPILLANTINI, MG ;
CROWTHER, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (05) :1983-1987
[23]   CLONING AND SEQUENCING OF THE CDNA-ENCODING AN ISOFORM OF MICROTUBULE-ASSOCIATED PROTEIN TAU CONTAINING 4 TANDEM REPEATS - DIFFERENTIAL EXPRESSION OF TAU PROTEIN MESSENGER-RNAS IN HUMAN-BRAIN [J].
GOEDERT, M ;
SPILLANTINI, MG ;
POTIER, MC ;
ULRICH, J ;
CROWTHER, RA .
EMBO JOURNAL, 1989, 8 (02) :393-399
[24]   TAU CONSISTS OF A SET OF PROTEINS WITH REPEATED C-TERMINAL MICROTUBULE-BINDING DOMAINS AND VARIABLE N-TERMINAL DOMAINS [J].
HIMMLER, A ;
DRECHSEL, D ;
KIRSCHNER, MW ;
MARTIN, DW .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (04) :1381-1388
[25]   STRUCTURE OF THE BOVINE TAU-GENE - ALTERNATIVELY SPLICED TRANSCRIPTS GENERATE A PROTEIN FAMILY [J].
HIMMLER, A .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (04) :1389-1396
[26]   OVEREXPRESSION OF TAU IN A NONNEURONAL CELL INDUCES LONG CELLULAR PROCESSES [J].
KNOPS, J ;
KOSIK, KS ;
LEE, G ;
PARDEE, JD ;
COHENGOULD, L ;
MCCONLOGUE, L .
JOURNAL OF CELL BIOLOGY, 1991, 114 (04) :725-733
[27]   DEVELOPMENTALLY REGULATED EXPRESSION OF SPECIFIC TAU SEQUENCES [J].
KOSIK, KS ;
ORECCHIO, LD ;
BAKALIS, S ;
NEVE, RL .
NEURON, 1989, 2 (04) :1389-1397
[28]   THE PRIMARY STRUCTURE AND HETEROGENEITY OF TAU-PROTEIN FROM MOUSE-BRAIN [J].
LEE, G ;
COWAN, N ;
KIRSCHNER, M .
SCIENCE, 1988, 239 (4837) :285-288
[29]   THE MICROTUBULE BINDING DOMAIN OF TAU-PROTEIN [J].
LEE, G ;
NEVE, RL ;
KOSIK, KS .
NEURON, 1989, 2 (06) :1615-1624
[30]  
LEE G, 1992, J CELL SCI, V102, P227