Cooperative Function of POU Proteins and SOX Proteins in Glial Cells

Glial cells of the oligodendrocyte lineage express several highly related POU proteins including Tst-1/Oct6/SCIP and Brn-1. Tst-1/Oct6/SCIP, but not Brn-1 efficiently cooperated with Sox10, the only SRY box protein so far identified in oligodendrocytes. Here we show that, in addition to Sox10, cells...

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Bibliographic Details
Published in:The Journal of biological chemistry 1998-06, Vol.273 (26), p.16050-16057
Main Authors: Kuhlbrodt, K, Herbarth, B, Sock, E, Enderich, J, Hermans-Borgmeyer, I, Wegner, M
Format: Article
Language:English
Subjects:
Amino Acid Sequence
Animals
COS Cells
Drug Synergism
High Mobility Group Proteins - physiology
Mice
Molecular Sequence Data
Nerve Tissue Proteins
Neuropeptides - physiology
Oligodendroglia - physiology
POU Domain Factors
Rats
Rats, Wistar
SOXC Transcription Factors
Trans-Activators - physiology
Transcriptional Activation
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Summary:Glial cells of the oligodendrocyte lineage express several highly related POU proteins including Tst-1/Oct6/SCIP and Brn-1. Tst-1/Oct6/SCIP, but not Brn-1 efficiently cooperated with Sox10, the only SRY box protein so far identified in oligodendrocytes. Here we show that, in addition to Sox10, cells of the oligodendrocyte lineage contain significant amounts of the related SRY box proteins Sox4 and Sox11. During development, Sox11 was strongly expressed in the central nervous system. It was first detected in neural precursors throughout the neuroepithelium. During later stages of neural development, Sox11 was additionally expressed in areas of the brain in which neurons undergo differentiation. In agreement with its expression in neural precursors, Sox11 levels in cells of the oligodendrocyte lineage were high in precursors and down-regulated during terminal differentiation. Outside the nervous system, expression of Sox11 was also detected in the developing limbs, face, and kidneys. Structure function analysis revealed that Sox11 has a strong intrinsic transactivation capacity which is mediated by a transactivation domain in its carboxyl-terminal part. In addition, Sox11 efficiently synergized with Brn-1. Synergy was dependent on binding of both proteins to adjacent DNA elements, and required the presence of the respective transactivation domain in each protein. Our data suggest the existence of a specific code in which POU proteins require specific Sox proteins to exhibit cooperative effects in glial cells.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.273.26.16050