Abstract

The maize karyotype was first characterized by the observation of pachytene chromosomes. The somatic chromosomes were identified by C-banding and FISH with repetitive DNA sequences. C-banding was useful for the identification of chromosome abnormalities in callus cultures. In the present review, we focus on the involvement of heterochromatic knobs on the occurrence of chromosome abnormalities in callus cultures. In a previous work we detected anaphase bridges resulting from delayed chromatid separation at knob regions and typical bridges derived from dicentric chromatids in cultures. The analysis of altered chromosomes showed they were derived from a chromatid-type breakage-fusion-bridge (BFB) cycle. Fluorescent in situ hybridization (FISH) showed signals of telomere sequences in the broken chromosome arm, thus giving evidence of de novo telomere formation on the broken chromosome end. Further observations of long- and short-term cultures have shown the presence of chromosome alterations derived from BFB cycles followed by chromosome healing. Additionally, the occurrence of unequal crossing over in a knob region was observed in callus culture. These results are of interest for studies on the mechanisms of chromosome alterations during evolution.

Highlights

  • Maize is an important crop plant and model organism

  • The maize karyotype was first characterized by the observation of pachytene chromosomes obtained from pollen mother cells, since the pioneering work by McClintock [1]

  • We focus on the involvement of heterochromatic knobs on the occurrence of chromosome abnormalities in maize callus cultures

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Summary

Introduction

Maize is an important crop plant and model organism. The maize karyotype was first characterized by the observation of pachytene chromosomes obtained from pollen mother cells, since the pioneering work by McClintock [1]. Structures containing heterochromatin were described: heterochromatic knobs, centromeric heterochromatin, B chromosomes, abnormal chromosome 10, and nucleolus organizer region localized on chromosome 6 [6]. The somatic chromosomes were identified by the C-banding procedure which was useful for the identification of chromosomal abnormalities in callus cultures [8–10]. We focus on the involvement of heterochromatic knobs on the occurrence of chromosome abnormalities in maize callus cultures. One genetic effect attributed to knobs is their influence on recombination [6, 19], and it was revealed that knobs in heterozygous condition can reduce local recombination [19] Another interesting genetic effect of knobs is their activity as neocentromeres resulting in meiotic drive. The effect of knobs on chromosome break and origin of abnormalities in maize callus culture is presented in this review

Heterochromatin involvement in chromosome breakage
Breakage-fusion-bridge cycle in callus culture and de novo telomere formation
Chromosome 7 and 9 abnormalities in long-term subcultures
Findings
Conclusions

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