We have developed from crosses of oat (Avena sativa L.) and maize (Zea mays L.) 50 fertile lines that are disomic additions of individual maize chromosomes 1-9 and chromosome 10 as a short-arm telosome. The whole chromosome 10 addition is available only in haploid oat background. Most of the maize chromosome disomic addition lines have regular transmission; however, chromosome 5 showed diminished paternal transmission, and chromosome 10 is transmitted to offspring only as a short-arm telosome. To further dissect the maize genome, we irradiated monosomic additions with ␥ rays and recovered radiation hybrid (RH) lines providing low-to medium-resolution mapping for most of the maize chromosomes. For maize chromosome 1, mapping 45 simple-sequence repeat markers delineated 10 groups of RH plants reflecting different chromosome breaks. The present chromosome 1 RH panel dissects this chromosome into eight physical segments defined by the 10 groups of RH lines. Genomic in situ hybridization revealed the physical size of a distal region, which is represented by six of the eight physical segments, as being Ϸ20% of the length of the short arm, representing Ϸone-third of the genetic chromosome 1 map. The distal Ϸ20% of the physical length of the long arm of maize chromosome 1 is represented by a single group of RH lines that spans >23% of the total genetic map. These oat-maize RH lines provide valuable tools for physical mapping of the complex highly duplicated maize genome and for unique studies of interspecific gene interactions. P lants with one chromosome (monosomic) or one pair of homologous chromosomes (disomic) of an alien donor species added to the entire recipient species chromosome complement serve to dissect the donor genome into individual chromosome entities and separate them from their own genome remnant. The transfer liberates the added chromosome (pair) from the interactive gene expression network of the donor genome and puts the chromosome's genes into the environment of the host genome. This new structural and functional situation can create novel orthologous and nonhomologous gene-to-gene interactions and, hence, helps to answer fundamental questions about gene expression control, inheritance, and syntenic correspondence among different plant species, especially those with large genomes, including maize, with a 1C content of Ϸ2. By crossing maize to oat, (oat ϫ maize)F 1 proembryos were generated, of which 5-10% could be rescued in vitro. Molecular and cytological analyses showed retention of one or more maize chromosomes in addition to the haploid oat genome in 34% of the F 1 plants (2-7). Because haploid oat frequently develops unreduced gametes (8), subsequent self-fertilization of (oat ϫ maize)F 1 plants with one maize chromosome added to the haploid oat genome (n ϭ 3x ϩ 1 ϭ 22) can produce F 2 offspring with one homologous maize chromosome pair added to the doubled haploid (hexaploid) oat genome (2n ϭ 6x ϩ 2 ϭ 44) among other euploid and aneuploid types (9).A complete series of oat-maize chromosome a...