mab-2 encodes RNT-1, a C. elegans Runx homologue essential for controlling cell proliferation in a stem cell-like developmental lineage

• Published in: Development (Cambridge) Vol. 132; no. 22; pp. 5043 - 5054
• Main Authors: Nimmo, Rachael, Antebi, Adam, Woollard, Alison
• Format: Journal Article
• Language: English
• Published: England The Company of Biologists Limited 01.11.2005
• Subjects: Animals; Caenorhabditis elegans - cytology; Caenorhabditis elegans - genetics; Caenorhabditis elegans - physiology; Caenorhabditis elegans Proteins - genetics; Caenorhabditis elegans Proteins - physiology; Cell Lineage - physiology; Cell Proliferation; Core Binding Factor alpha Subunits - genetics; Female; Male; RNA Interference; Stem Cells - cytology; Stem Cells - physiology; Transcription Factors - genetics; Transcription Factors - physiology
• ISSN: 0950-1991; 1477-9129
• DOI: 10.1242/dev.02102

In this report, we demonstrate that C. elegans mab-2 mutants have defects in the development of a male-specific sense organ because of a failure in the proliferation of the stem cell-like lateral hypodermal (seam) cells. We show, by positional cloning, that mab-2 encodes RNT-1, the only C. elegans member of the Runx family of transcriptional regulators, which are postulated to act both as oncogenes and tumour suppressors in mammalian cells. Importantly, we find that rnt-1 is a rate-limiting regulator of seam cell proliferation in C. elegans , as overexpression of rnt-1 at particular developmental stages is capable of driving extra cell divisions, leading to seam cell hyperplasia. Loss of rnt-1 is correlated with upregulation of cki-1 , a CDK inhibitor. Deregulated expression of Runx genes in humans is associated with various cancers, particularly leukaemias, suggesting a conserved role for Runx genes in controlling cell proliferation during development, especially in stem cell lineages. C. elegans is therefore an important model system for studying the biology, and oncogenic potential, of Runx genes.