Key points are not available for this paper at this time.
Answers are grounded in this paper and cite their sources.
LIM as metallodomain may enable redox-sensitive transcription; leaves open in vivo roles in cell lineage and mammalian homologs.
The cysteine-rich LIM motif is highly conserved between invertebrates and mammals. This motif shows similarity both to proteins that bind zinc and to ferredoxins, which contain iron-sulfur clusters. Two tandem copies of the LIM motif are found in a number of presumptive transcription factors, including the protein product of the Caenorhabditis elegans cell-lineage gene lin-11. To investigate the possible metal-binding properties of the LIM region of the lin-11 protein, we expressed and purified a 151-amino acid peptide containing the tandem LIM motifs. The purified peptide binds both zinc (two atoms per protein molecule) and iron (as a redox-active iron-sulfur cluster, with four atoms of iron and four atoms of inorganic sulfide per protein molecule). These observations suggest that the LIM motif is a metallodomain that might function in a redox-sensitive regulation of transcription.
No takes yet. Share an insight, caveat, or question.
Li et al. (1991) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: