Potato (Solanum tuberosum) homeobox 1 (POTH1) is a class I homeobox gene isolated from an early-stage tuber cDNA library. The RNA expression pattern of POTH1, unlike that of most other class I knotted-like homeobox genes, is widespread in the cells of both indeterminate and differentiated tissues. Using in situ hybridization, POTH1 transcripts were detected in meristematic cells, leaf primordia, and the vascular procambium of the young stem. Overexpression of POTH1 produced dwarf plants with altered leaf morphology. Leaves were reduced in size and displayed a "mouse-ear" phenotype. The mid-vein was less prominent, resulting in a palmate venation pattern. The overall plant height of overexpression lines was reduced due to a decrease in internode length. Levels of intermediates in the gibberellin (GA) biosynthetic pathway were altered, and the bioactive GA, GA 1 , was reduced by one-half in sense mutants. Accumulation of mRNA for GA 20-oxidase1, a key biosynthetic enzyme, decreased in overexpression lines. In vitro tuberization was enhanced under both short-and long-day photoperiods in several POTH1 overexpression lines. Sense lines produced more tubers at a faster rate than controls. These results imply that POTH1 mediates the development of potato by acting as a negative regulator of GA biosynthesis.Homeobox genes, a family of transcription factors highly conserved in animals, plants, and yeast (Chan et al., 1998), are implicated in the control of cell fate. The Antennapedia homeobox gene in fruitfly (Drosophila melanogaster), for example, specifies leg identity while inhibiting the formation of an antenna (Mann and Chan, 1996). Ectopic expression of the eyeless gene in the wing imaginal disc tissue of fruitfly embryos causes a normal eye to form on the wings (Halder et al., 1995). The first plant homeobox gene to be discovered was knotted1 (kn1) from maize (Zea mays; Vollbrecht et al., 1991). Dominant gain-offunction mutations of Kn1 formed knot-like structures along lateral veins. These knots were composed of cells that continued to divide rather than differentiate normally (Vollbrecht et al., 1991;Smith et al., 1992), indicating that kn1 is involved in regulating cell fate (Clark et al., 1996; Kerstetter et al., 1997; Chan et al., 1998).Knotted-like homeobox (knox) genes have been isolated from several plant species (for review, see Reiser et al., 2000) and can be divided into two classes based on expression patterns and sequence similarity (Kerstetter et al., 1994). Class I knox genes have high similarity to the kn1 homeodomain and generally have a meristem-specific mRNA expression pattern. Class II knox genes usually have a more widespread expression pattern. Knox genes are members of the three amino acid loop extension (TALE) superclass of homeobox genes (Bü rglin, 1997). The TALE superclass includes members from plants, animals, and fungi and is characterized by the addition of three amino acids, Pro-Tyr-Pro (PYP), between helices 1 and 2 of the homeodomain. Knox genes share conserved regions outside of...