Assay of centromere function using a human artificial chromosome

• Published in: Chromosoma Vol. 107; no. 6-7; pp. 406 - 416
• Main Authors: Masumoto, H, Ikeno, M, Nakano, M, Okazaki, T, Grimes, B, Cooke, H, Suzuki, N
• Format: Journal Article
• Language: English
• Published: Austria Springer Nature B.V 01.12.1998
• Subjects: Artificial chromosomes; Autoantigens; Cells, Cultured; Centromere - physiology; Centromere Protein B; Chromosomal Proteins, Non-Histone - physiology; Chromosome Segregation; Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 21 - physiology; Cloning, Molecular; DNA-Binding Proteins; Genetics; Humans; In Situ Hybridization, Fluorescence; Kinetochores; Nuclear Proteins; Repetitive Sequences, Nucleic Acid; Spindle Apparatus; Telomere; Transfection
• DOI: 10.1007/s004120050324
• ISSN: 0009-5915

In order to define a functional human centromere sequence, an artificial chromosome was constructed as a reproducible DNA molecule. Mammalian telomere repeats and a selectable marker were introduced into yeast artificial chromosomes (YACs) containing alphoid DNA from the centromere region of human chromosome 21 in a recombination-deficient yeast host. When these modified YACs were introduced into cultured human cells, a YAC with the alphoid DNA from the alpha21-I locus, containing CENP-B boxes at a high frequency and a regular repeat array, efficiently formed minichromosomes that were maintained stably in the absence of selection and bound CENP-A, CENP-B, CENP-C and CENP-E. The minichromosomes, 1-5 Mb in size and composed of multimers of the introduced YAC DNA, aligned at metaphase plates and segregated to opposite poles correctly in anaphase. Extensive cytological analyses strongly suggested that the minichromosomes had not acquired host sequences and were formed in all cases by a de novo mechanism. In contrast, minichromosomes were never produced with a modified YAC containing alphoid DNA from the alpha21-II locus, which contains no CENP-B boxes and has a less regular sequence arrangement. We conclude that alpha21-I alphoid DNA can induce de novo assembly of active centromere/kinetochore structures on minichromosomes.