Abstract

LIM homeodomain transcription factors regulate development in complex organisms. To characterize the molecular signals required for the nuclear localization of these proteins, we examined the Lhx3 factor. Lhx3 is essential for pituitary organogenesis and motor neuron specification. By using functional fluorescent derivatives, we demonstrate that Lhx3 is found in both the nucleoplasm and nuclear matrix. Three nuclear localization signals were mapped within the homeodomain, and one was located in the carboxyl terminus. The homeodomain also serves as the nuclear matrix targeting sequence. No individual signal is alone required for nuclear localization of Lhx3; the signals work in combinatorial fashion. Specific combinations of these signals transferred nuclear localization to cytoplasmic proteins. Mutation of nuclear localization signals within the homeodomain inhibited Lhx3 transcriptional function. By contrast, mutation of the carboxyl-terminal signal activated Lhx3, indicating that this region is critical to transcriptional activity and may be a target of regulatory pathways. The pattern of conservation of the nuclear localization and nuclear matrix targeting signals suggests that the LIM homeodomain factors use similar mechanisms for subcellular localization. Furthermore, upon nuclear entry, association of Lhx3 with the nuclear matrix may contribute to LIM homeodomain factor interaction with other classes of transcription factors.

Highlights

  • A family of homeodomain transcription factors, initially named for three members, shares a cysteine-rich domain containing two zinc-coordinated structures, referred to as the LIM domain (1, 2)

  • It has been suggested that transcriptionally active genes are associated with the nuclear complex; NLS, nuclear localization signal; EGFP, enhanced green fluorescent protein; GSU, ␣ glycoprotein subunit; Electrophoretic mobility shift assays (EMSA), electrophoretic mobility shift assays; DAPI, 4Ј,6-diamidino-2-phenylindole dihydrochloride; PBS, phosphate-buffered saline; TSH, thyroid-stimulating hormone

  • The identified nuclear localization sequences are conserved within the Lhx3 family of proteins and in LIM homeodomain (LIM-HD) proteins in general, suggesting that other LIM-HD proteins that serve as essential developmental transcription factors may use similar complex signals for nuclear translocation

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Summary

Introduction

A family of homeodomain transcription factors, initially named for three members (lin-11, Isl-1, and mec-3), shares a cysteine-rich domain containing two zinc-coordinated structures, referred to as the LIM domain (1, 2). To investigate the mechanism by which LIM-HD proteins enter the cell nucleus, the signals required for nuclear entry and nuclear matrix association of the Lhx3 LIM-HD molecule ( known as P-Lim/LIM-3) were characterized. The identified nuclear localization sequences are conserved within the Lhx3 family of proteins and in LIM-HD proteins in general, suggesting that other LIM-HD proteins that serve as essential developmental transcription factors may use similar complex signals for nuclear translocation.

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