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1.
Figure 1

Figure 1. Dot-plot comparison of nucleotide sequences of human and mouse X chromosomes reveals large, divergent ampliconic regions on mouse X chromosome. From: Independent specialization of the human and mouse X chromosomes for the male germline.

Dot plot generated from BLASTZ nucleotide alignments of the human X chromosome assembly, prior to our SHIMS refinement (vertical axis), and the single-haplotype mouse X chromosome assembly (horizontal axis); each dot represents >70% nucleotide identity, within a 10-kb window, at that position. Within the plot, diagonal lines indicate syntenic blocks between the two chromosomes; regions lacking such diagonals are comprised of species-specific sequences. Blue shading highlights divergent ampliconic regions, each >500 kb in length, on the mouse X chromosome.

Jacob L. Mueller, et al. Nat Genet. ;45(9):1083-1087.
2.
Figure 3

Figure 3. Comparison of X-linked gene classes between human and mouse. From: Independent specialization of the human and mouse X chromosomes for the male germline.

a, At center, Venn diagram depicts all human and mouse X-linked genes that are shared or not shared. To left and right, pie charts depict species-specific genes independently acquired in that lineage (blue), duplicated from an ancestral X-linked gene in that lineage (light gray), or lost in the opposite lineage (light gray). Venn diagram and pie charts are drawn to scale (by gene number). b, Horizontal bar stacks of single-copy, multicopy and ampliconic genes shared (dark gray) and independently acquired (blue) on human and mouse X chromosomes. Bar stacks are to scale (by gene number). c, Percentages of genes expressed predominantly in testis and in testicular germ cells. Horizontal dotted lines represent percentages of autosomal genes exhibiting testis- or testicular-germ-cell-predominant expression. SC, single-copy; MC, multicopy; AMP, ampliconic. Each asterisk indicates Chi-square test with Yates’ correction p < 0.0001 (degrees of freedom = 1) when compared to either autosomal genes or X-linked single-copy genes.

Jacob L. Mueller, et al. Nat Genet. ;45(9):1083-1087.
3.
Figure 2

Figure 2. Comparison of mosaic and SHIMS sequence assemblies across one region of human X chromosome. From: Independent specialization of the human and mouse X chromosomes for the male germline.

a, Triangular dot-plot highlights sequence similarities within mosaic (multi-haplotype) assembly. Each dot represents 100% identity within a window of 100 nucleotides; direct repeats appear as horizontal lines, inverted repeats as vertical lines, and palindromes as vertical lines that nearly intersect the baseline; gaps are indicated by gray shading. Black arrows immediately below plots denote positions and orientations of amplicons. Further below, sequenced BACs from CTD, RP-11, and RP-13 libraries (each from a different individual) contributing to the assembly are depicted as orange, green, and purple bars, respectively; each bar reflects extent and position within assembly of finished sequence for that BAC. (As per the human genome assembly standard, finished-sequence overlaps between adjoining BACs are limited to 2 kb.) GenBank accession numbers in Supplementary Table 1. b, SHIMS assembly of same region. All BACs derive from RP-11 library (one male) and are fully sequenced; each BAC’s finished sequence extensively overlaps those of adjoining BACs.

Jacob L. Mueller, et al. Nat Genet. ;45(9):1083-1087.

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