Title

Dynamic expression of LIM cofactors in the developing mouse neural tube

UMMS Affiliation

Programs in Gene Function and Expression; Program in Molecular Medicine

Publication Date

1-6-2006

Document Type

Article

Subjects

Animals; Central Nervous System; DNA-Binding Proteins; Homeodomain Proteins; Metalloproteins; Mice; RNA, Messenger; Repressor Proteins; Transcription Factors

Disciplines

Genetics and Genomics

Abstract

The developmental regulation of LIM homeodomain transcription factors (LIM-HD) by the LIM domain-binding cofactors CLIM/Ldb/NLI and RLIM has been demonstrated. Whereas CLIM cofactors are thought to be required for at least some of the in vivo functions of LIM-HD proteins, the ubiquitin ligase RLIM functions as a negative regulator by its ability to target CLIM cofactors for proteasomal degradation. In this report, we have investigated and compared the protein expression of both factors in the developing mouse neural tube. We co-localize both proteins in many tissues and, although widely expressed, we detect high levels of both cofactors in specific neural tube regions, e.g., in the ventral neural tube, where motor neurons reside. The mostly ubiquitous distribution of RLIM- and CLIM-encoding mRNA differs from the more specific expression of both cofactors at the protein level, indicating post-transcriptional regulation. Furthermore, we show that both cofactors not only co-localize with each other but also with Isl and Lhx3 LIM-HD proteins in developing ventral neural tube neurons. Our results demonstrate the dynamic expression of cofactors participating in the regulation of LIM-HD proteins during the development of the neural tube in mice and suggest additional post-transcriptional regulation in the nuclear LIM-HD protein network.

DOI of Published Version

10.1002/dvdy.20669

Source

Dev Dyn. 2006 Mar;235(3):786-91. Link to article on publisher's site

Journal/Book/Conference Title

Developmental dynamics : an official publication of the American Association of Anatomists

Related Resources

Link to Article in PubMed

PubMed ID

16395690

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