The <i>LS</i> locus of pea encodes the gibberellin biosynthesis enzyme <i>ent</i>‐kaurene synthase A

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<jats:title>Summary</jats:title><jats:p>Gibberellins (GAs) are hormones required for several aspects of plant development, including internode elongation and seed development in pea (<jats:italic>Pisum sativum</jats:italic> L.). The first committed step in the GA biosynthesis pathway is the conversion of geranylgeranyl diphosphate (GGDP) to <jats:italic>ent</jats:italic>‐kaurene via copalyl diphosphate (CDP). These two reactions are catalyzed by the cyclases <jats:italic>ent</jats:italic>‐kaurene synthase A (KSA) and <jats:italic>ent</jats:italic>‐kaurene synthase B (KSB), respectively. Previous genetic and biochemical analysis of the GA‐responsive <jats:italic>ls‐1</jats:italic> mutant of pea suggested that GA levels are reduced in a developmental‐ and organ‐specific manner due to reduced GA biosynthesis. Analysis of cell‐free enzyme preparations from WT and <jats:italic>ls‐1</jats:italic> embryos at contact point reveals that <jats:italic>ls‐1</jats:italic> reduces the activity of KSA but not KSB. To characterize the <jats:italic>ls‐1</jats:italic> mutation in more detail, a cDNA coding for a pea KSA was cloned and shown to be encoded by the <jats:italic>LS</jats:italic> locus. The <jats:italic>ls‐1</jats:italic> mutation results from an intronic G to A substitution that causes impaired RNA splicing. To determine the activity of the KSAs encoded by the <jats:italic>LS</jats:italic> and <jats:italic>ls‐1</jats:italic> alleles, a new <jats:italic>in vitro</jats:italic> assay for combined KSA and KSB activity has been developed using the KSB gene of pumpkin. Using recombinant WT KSA and KSB fusion proteins, GGDP is converted to <jats:italic>ent</jats:italic>‐kaurene <jats:italic>in vitro</jats:italic>. Based on the sequence of RT‐PCR products, three different truncated KSA proteins are predicted to exist in <jats:italic>ls‐1</jats:italic> plants. The most abundant mutant KSA protein does not possess detectable activity <jats:italic>in vitro</jats:italic>. Nevertheless, the <jats:italic>ls‐1</jats:italic> allele is not null and is able to encode at least a partially functional KSA since a more severe <jats:italic>ls</jats:italic> allele has been identified. The <jats:italic>ls‐1</jats:italic> mutation has played a key role in identifying a role for GAs in pea seed development in the first few days after fertilization, but not in older seeds. KSA expression in seeds is developmentally regulated and parallels overall GA biosynthesis, suggesting that KSA expression may play an important role in the regulation of GA biosynthesis and seed development.</jats:p>

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