The null wx-ml allele contains a 409-bp Dissociation 1 (Dsl) element in exon 9 of the maize waxy (Wx) gene. In the absence of the autonomous Activator (Ac) element, the Dsl element cannot transpose, and this allele encodes several Wx transcripts that arise following alternative splicing of Dsl sequences from Wx pre-mRNA. Splicing involves the utilization of three 5' splice sites and three 3' splice sites. All but one of these splice sites are in Dsl sequences near the ends of the element. The presence of 5' and 3' splice sites near the Dsl termini and the element's small size and AT richness are features that distinguish Dsl elements from all other known Ds elements. It is suggested that these features may enhance the ability of Dsl to function as a mobile intron.The insertion of maize transposable elements into genes does not always abolish gene expression. Certain Dissociation (Ds)-and defective-suppressor-mutator (dSpm)-containing alleles of the maize alcohol dehydrogenase 1 (AdhilFm335), waxy (wx-m9), and bronze (bz-m13, bz-m13CS9) genes display a stable intermediate or nonmutant phenotype in strains in which these elements cannot transpose, that is, in the absence of the autonomous Activator (Ac) or Spm element (16,19,21,24). In addition to these examples, the null Ds alleles wx-B4 and AdhJ-2FJJ encode non-mutantsize Wx or Adhl transcripts (5,32). Surprisingly, molecular cloning and DNA sequence analysis revealed that these leaky and null alleles contain exon insertions and that all, except Adhi-Fm335, contain insertions in translated exons (5,6,24,27,32).To understand how genes containing large transposable elements in translated exons can encode functional products, wild-type-size products or both, we have focused on several Ds alleles of the waxy (Wx) gene. Wx encodes a starch granule-bound ADP-glucose glucosyl transferase that is responsible for amylose biosynthesis in the endosperm and pollen (20). The leaky wx-m9 allele and the null wx-B4 allele encode non-mutant-size Wx mRNAs, despite the presence of 4.3-and 1.4-kb Ds elements, respectively, in translated exons (32). For both alleles, the Ds elements can be alternatively spliced from pre-mRNAs if one of three 5' splice sites clustered within 20 bp near the Ds terminus is joined to a 3' splice site within the Wx gene adjacent to the Ds element (32). None of the resultant Wx mRNAs are wild type, because part of the Ds terminus remains in the mature message.The splicing of the Ds insertion of the wx-ml allele is the focus of this report. Like wx-B4, this allele is null in the absence of Ac (14). The Ds insertion in wx-ml is in exon 9, is 409 bp in length, and is a Ds]-type element (33). Unlike the 4.3-kb Ds of wx-m9 and the 1.4-kb Ds of wx-B4, which are deletion derivatives of the Ac element (6, 29), DsJ elements share only about 40 bp of homology with Ac sequences (22,27). This 40 bp includes the 11-bp inverted repeats and most of the 20 bp adjacent to one terminus that contains the cluster of 5' splice sites involved in Ds processing. Dennis et al. (4...