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. 2016 Nov 28;5:e19090. doi: 10.7554/eLife.19090

Figure 2. MIC chromosome landscapes.

For each chromosome, the top panel shows the density of several genomic features, measured as number of base pairs (span) per 500 kb sliding window (100 kb slide increment). Purple = simple sequence repetitive DNA (note that exclusion of those simple sequence repeats that overlap with TEs has minimal effect on the distribution pattern). Blue = putative TEs. Green = high-confidence IESs. Orange = protein-coding sequences. The corresponding chromosome-length super-assembly (Super-Asm) is shown immediately below, each Cbs indicated by a vertical tick. Red ticks indicate Cbs’s flanking putative centromeres (see main text and Figure 2—figure supplement 1). In the 'MIC-scaff' schematic, the scaffolds comprising each MIC chromosome super-assembly are depicted as horizontal lines (alternating in vertical position to delineate each from its neighbors). The ‘MAC-scaff’ schematic indicates the positions of MAC scaffolds (many of which are complete, fully sequenced MAC chromosomes) derived from the corresponding regions of the MIC chromosome. Note that, because IESs are absent from MAC scaffolds, their lengths are actually shorter, but for simplicity of viewing, these lengths have been stretched so that MAC-scaff endpoints line up with their corresponding positions in the MIC. Chromosomes are stacked so that their centers align vertically.

DOI: http://dx.doi.org/10.7554/eLife.19090.004

Figure 2.

Figure 2—figure supplement 1. Deletion mapping of Tetrahymena centromeres.

Figure 2—figure supplement 1.

In a separate study, Cassidy-Hanley et al. isolated a collection of strains carrying partial or complete MIC chromosomal deletions. Such deletions are viable because their expressed MAC contains the complete genome. MIC chromosomes are transcriptionally silent, but deletions that mitotically destabilize a chromosome by compromising centromere function would not be recovered. We mapped the extent of the deletions relative to Cbs’s spread along the length of each MIC chromosome. The figure shows mapping of Chromosome 5 deletions as a representative example. The extents of left arm deletions are indicated by orange lines; right arm deletions by blue lines. Six independent deletions removed all the Cbs’s on the left arm while three others removed all the Cbs’s on the right arm (the precise endpoints have not yet been mapped, as indicated by the dotted line termini). Five arm-specific, smaller deletions were also mapped, as shown. Only whole chromosome deletions were recovered that removed both Cbs 5L1 and Cbs 5R1, marked in red, as in Figure 2. We infer that sequences essential for centromere function lie between these two Cbs’s.