Although the centromeres of some plants have been investigated previously, our knowledge of the wheat centromere is still very limited. To understand the structure and function of the wheat centromere, we used two centromeric repeats (RCS1 and CCS1-5ab) to obtain some centromere-associated bacterial artificial chromosome (BAC) clones in 32 RCS1-related BAC clones that had been screened out from a diploid wheat (Triticum boeoticum Boiss.; 2n=2x=14) BAC library. Southern hybridization results indicated that, of the 32 candidates, there were 28 RCS1-positive clones. Based on gel blot patterns, the frequency of RCS1 was approximately one copy every 69.4 kb in these 28 RCS1-positive BAC clones. More bands were detected when the same filter was probed with CCS1-5ab. Furthermore, the CCS1 bands covered all the bands detected by RCS1, which suggests that some CCS1 repeats were distributed together with RCS1. The frequency of CCS1 families was once every 35.8 kb, nearly twice that of RCS1. Fluorescence in situ hybridization (FISH) analysis indicated that the five BAC clones containing RCS1 and CCS1 sequences all detected signals at the centromeric regions in hexaploid wheat, but the signal intensities on the A-genome chromosomes were stronger than those on the B-and/or Dgenome chromosomes. The FISH analysis among nine Triticeae cereals indicated that there were A-genomespecific (or rich) sequences dispersing on chromosome arms in the BAC clone TbBAC5. In addition, at the interphase cells, the centromeres of diploid species usually clustered at one pole and formed a ring-like allocation in the period before metaphase. Centromeres play critical roles in the faithful segregation of sister chromatids during the period of mitosis and meiosis (Presting et al. 1998;Jin et al. 2004). Although they have the same function, the DNA sequences of centromeric regions are not conserved among species (Clarke 1990;Houben and Schubert 2003;Ito et al. 2004;Jin et al. 2004). Owing to highly heterochromatic structure and complex repeats, it is more difficult to clone, map, sequence, and assemble the centromeres than the low-copy number DNA. Therefore, the centromere has become the last barrier of entire genome sequencing at present (Zhang et al. 2004b).In plants, considerable achievements have been made with regard to centromeres of model plants over the past few years. Highly repetitive "satellite" arrays and dispersed transponsable elements have been detected in most centromeres studied, where the former is organized into long stretches, interrupted by the latter and located at the core region . Studies have shown that the centromeres of Arabidopsis thaliana consist of a 178 ± 1 bp pAL1 satellite and Athila retroelement (Copenhaver et al. 1999;Houben and Schubert 2003). In rice (Oryza sativa L.), the DNA sequences in centromeres are composed of 155/156 bp CentO satellite and Centromeric Retrotransposon of BAC Clones Associated with Wheat Centromeres 349 Rice (CRR; Dong et al. 1998;Cheng et al. 2002;Jiang et al. 2003;Zhang et al. 20...