EXPRESSION OF MYELIN TRANSCRIPTION FACTOR-I (MYTI), A ZINC-FINGER DNA-BINDING PROTEIN, IN DEVELOPING OLIGODENDROCYTES

被引:76
作者
ARMSTRONG, RC [1 ]
KIM, JG [1 ]
HUDSON, LD [1 ]
机构
[1] NINCDS,DEV NEUROGENET LAB,BETHESDA,MD 20892
关键词
GLIA; GENE REGULATION; MYELINATION; PROTEOLIPID PROTEIN;
D O I
10.1002/glia.440140407
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The production of myelin by oligodendrocytes requires the coordinated, massive synthesis of myelin components, a program that is dependent on transcriptional controls. Myelin transcription factor I (MyTI) was named for its ability to recognize the proteolipid protein (PLP) gene, the most abundantly transcribed central nervous system myelin gene (Kim and Hudson: Mol. Cell Biol. 12:5632, 1992). MyTI is a zinc-dependent, DNA-binding protein of the Cys(2)-His-Cys class. The pattern of MyTI expression, documented in the present study, suggests that MyTI may be instrumental in early stages of oligodendrocytic development and myelin production. MyTI mRNA transcripts are more highly expressed in oligodendrocyte progenitors than in differentiated oligodendrocytes. In vitro and in vivo analyses show that MyTI immunoreactivity is stronger in oligodendrocytic progenitors than in mature oligodendrocytes which have already accumulated PLP. In oligodendrocyte progenitors, MyTI immunoreactivity appears as speckles within the nucleus, suggestive of an association of MyTI with a function that is spatially segregated into discrete nuclear domains. MyTI continues to be expressed in cells transcribing PLP. However, as oligodendrocytes accumulate PLP, MyTI immunoreactivity becomes restricted to the cytoplasm and progressively diminishes. Since MyTI has two widely separated sets of DNA-binding domains and initial MyTI expression markedly precedes PLP expression, we hypothesize the following model: MyTI may play a role in assembling transcriptionally active complexes of PLP, perhaps by bending the DNA of the promoter region to induce an appropriate conformation to enable subsequent binding of additional regulatory proteins. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:303 / 321
页数:19
相关论文
共 71 条
[1]   INVITRO ANALYSIS OF THE OLIGODENDROCYTE LINEAGE IN MICE DURING DEMYELINATION AND REMYELINATION [J].
ARMSTRONG, R ;
FRIEDRICH, VL ;
HOLMES, KV ;
DUBOISDALCQ, M .
JOURNAL OF CELL BIOLOGY, 1990, 111 (03) :1183-1195
[2]   TYPE-1 ASTROCYTES AND OLIGODENDROCYTE-TYPE-2 ASTROCYTE GLIAL PROGENITORS MIGRATE TOWARD DISTINCT MOLECULES [J].
ARMSTRONG, RC ;
HARVATH, L ;
DUBOISDALCQ, ME .
JOURNAL OF NEUROSCIENCE RESEARCH, 1990, 27 (03) :400-407
[3]  
ARMSTRONG RC, 1994, INTRO STUDY ALCOHOL, P41
[4]   NOVEL STAGE IN THE OLIGODENDROCYTE LINEAGE DEFINED BY REACTIVITY OF PROGENITORS WITH R-MAB PRIOR TO O1 ANTI-GALACTOCEREBROSIDE [J].
BANSAL, R ;
PFEIFFER, SE .
JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 32 (03) :309-316
[5]  
BERNDT JA, 1992, J BIOL CHEM, V267, P14730
[6]   COOPERATION BETWEEN 2 GROWTH-FACTORS PROMOTES EXTENDED SELF-RENEWAL AND INHIBITS DIFFERENTIATION OF OLIGODENDROCYTE TYPE-2 ASTROCYTE (O-2A) PROGENITOR CELLS [J].
BOGLER, O ;
WREN, D ;
BARNETT, SC ;
LAND, H ;
NOBLE, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6368-6372
[7]   CHOLINE-ACETYLTRANSFERASE AND CALCITONIN GENE-RELATED PEPTIDE IMMUNOREACTIVITY IN MOTONEURONS AFTER DIFFERENT TYPES OF NERVE INJURY [J].
BORKE, RC ;
CURTIS, M ;
GINSBERG, C .
JOURNAL OF NEUROCYTOLOGY, 1993, 22 (03) :141-153
[8]   EXISTENCE OF 2 POPULATIONS OF CYCLIN PROLIFERATING CELL NUCLEAR ANTIGEN DURING THE CELL-CYCLE - ASSOCIATION WITH DNA-REPLICATION SITES [J].
BRAVO, R ;
MACDONALDBRAVO, H .
JOURNAL OF CELL BIOLOGY, 1987, 105 (04) :1549-1554
[9]  
BREITSCHOPF H, 1992, ACTA NEUROPATHOL, V84, P581
[10]   DM20 MESSENGER-RNA SPLICE PRODUCT OF THE MYELIN PROTEOLIPID PROTEIN GENE IS EXPRESSED IN THE MURINE HEART [J].
CAMPAGNONI, CW ;
GARBAY, B ;
MICEVYCH, P ;
PRIBYL, T ;
KAMPF, K ;
HANDLEY, VW ;
CAMPAGNONI, AT .
JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 33 (01) :148-155