Table 1.
Eukarya | Accession number | Category | Length [bp] | Correlation properties | ||||
---|---|---|---|---|---|---|---|---|
Start [N,R,P] [bp] | 1st max. [bp] | Transition [bp] | 2nd max. [F,R] [bp] | Fine-struc. [C,F] | ||||
Arabidopsis thaliana Chr. I top + bottom | AE00517 & AE005173 | P | 28,890,626 | P | 60/600 | 171 | 580 | C |
Arabidopsis thaliana Chr. I top | AE00517 | P | 14,221,746 | P | 60/550 | 160 | 550 | C |
Arabidopsis thaliana Chr. I bottom | AE005173 | P | 14,668,880 | P | 60/650 | 185 | 620 | C |
Arabidopsis thaliana Chr. II | AE002093 | P | 19,646,744 | P | 60/680 | 180 | 660 | C |
Arabidopsis thaliana Chr. IV | NC001268 | P | 17,549,956 | P | 60/650 | 160 | 680 | C |
Saccharomyces cerevisiae Chr. I | NC001133(1) | Y | 230,203 | P | 500 | – | – | C |
Saccharomyces cerevisiae Chr. II | NC001133(1) | Y | 813,139 | P | 435 | – | – | C |
Saccharomyces cerevisiae Chr. III | NC001133(2) | Y | 316,613 | P | 450 | – | – | C |
Saccharomyces cerevisiae Chr. IV | NC001133(2) | Y | 1,531,929 | P | 410 | – | – | C |
Saccharomyces cerevisiae Chr. V | NC001133(2) | Y | 576,870 | P | 640 | – | – | C |
Saccharomyces cerevisiae Chr. VI | NC001133(1) | Y | 270,148 | P | 640 | – | – | C |
Saccharomyces cerevisiae Chr. VII | NC001133(1) | Y | 1,090,936 | P | 540 | – | – | C |
Saccharomyces cerevisiae Chr. VIII | NC001133(2) | Y | 562,638 | P | 620 | – | – | C |
Saccharomyces cerevisiae Chr. IX | NC001133(1) | Y | 439,885 | P | 460 | – | – | C |
Saccharomyces cerevisiae Chr. X | NC001133(1) | Y | 745,440 | P | 460 | – | – | C |
Saccharomyces cerevisiae Chr. XI | NC001133(1) | Y | 666,445 | P | 580 | – | – | C |
Saccharomyces cerevisiae Chr. XII | NC001133(1) | Y | 1,078,173 | P | 560 | – | – | C |
Saccharomyces cerevisiae Chr. XIII | NC001133(1) | Y | 924,430 | P | 560 | – | – | C |
Saccharomyces cerevisiae Chr. XIV | NC001133(1) | Y | 784,330 | P | 450 | – | – | C |
Saccharomyces cerevisiae Chr. XV | NC001133(1) | Y | 1,091,284 | P | 550 | – | – | C |
Saccharomyces cerevisiae Chr. XVI | NC001133(1) | Y | 875,709 | P | 420 | – | – | C |
Schizosaccharomyces pombe Chr. I | V-011213 | Y | 5,602,103 | P | 900 | 1.2*^4 | R1.0*^5 | C |
Schizosaccharomyces pombe Chr. II | V-011213 | Y | 4,430,733 | P | 850 | 1.4*^4 | R1.0*^5 | C |
Schizosaccharomyces pombe Chr. III | V-011213 | Y | 2,467,649 | P | 610 | 2.0*^4 | R1.0*^5 | C |
Drosophila melanogaster Chr. 2L | 2L-1011210 | I | 2,265,1956 | P | 40/3,100 | – | – | C |
Drosophila melanogaster Chr. 2R | 2R-2-011210 | I | 14,631,223 | P | 40/3,800 | – | – | C |
Drosophila melanogaster Chr. 3R | 3R-1-011210 | I | 28,460,979 | P | 40/3,400 | – | – | C |
Homo sapiens sapiens Chr. XI | NT009151 | Pr | 19,322,668 | P | 200 | 1.0*^5 | R3.5*^5 | N |
Homo sapiens sapiens Chr. XIV | NT026437 | Pr | 28,334,988 | P | 200 | 1.7*^4 | F1.4*^5 | N |
Homo sapiens sapiens Chr. XV | NT010321 | Pr | 9,197,381 | P | 200 | 2.0*^4 | 1.0*^5 | N |
Homo sapiens sapiens Chr. XX | NT011362 | Pr | 24,982,240 | P | 200 | 1.2*^4 | 1.3*^5 | N |
Homo sapiens sapiens Chr. XXI | Hattori51 | Pr | 33820172 | P | 200 | 2.0*^4 | 1.3*^5 | N |
Homo sapiens sapiens Chr. XXII | TIGR, WLC010213 | Pr | 33,705,278 | P | 200 | 1.2*^4 | 2.0*^4 | N |
To simulate the whole chromosome I of Arabidopsis thaliana the sequences of the top and bottom arm that are separated by an unsequenced centromeric region were concatenated. Accession numbers of Saccharomyces cerevisiae are annotated with the version in brackets. The sequences of Schizosaccharomyces pombe are the preliminary from 10/12/2001. The sequences of Drosophila melanogaster are the three largest available sequences with “Gold Standard Quality” downloaded on 10/12/2001 from http://www.fruitfly.org/. A human sequence of chromosome XXI was used (Hattori et al. 2000) with no apparent accession number. The sequence of chromosome XXII was downloaded from The Institute for Genome Research (TIGR) website at http://www.tigr.org/. Taxonomic categories are plant (P), yeast (Y), insect (I), and primate (Pr). Properties of correlation are classified with N for negative (crossing the random regime with a value of 0.5 in bp), R for random, and P for positive correlation coefficients at window sizes of a few base pairs. The transition to the second maximum can be a minimum (M). Second maxima are dividable into those with a fine-structure not attributable to statistics (F) and those not clearly separable from fluctuations based on the cut-off length of sequences (R). The fine-structure is categorized by codon usage (C) and nucleosomal binding (N)