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Table 1 Analysis of test sequences with Locus-Assigner and RECCO.

From: Expression pattern analysis of transcribed HERV sequences is complicated by ex vivorecombination

1

2

3

4

5

6

7

8

9

artifical sequence

Locus-Assigner

# diff's

# recom's

loci involved

recom region

# diff's to locus

p value

# diff's after recom

B86_B107

22_012

37

1

22_012

7_450

282 – 307

4

0

0,001

4

B112_B131

7_450

34

1

7_450

6_324/3_496

282 – 307

1

0

0,001

1

B2_B15_B2

4_742

26

2

4_742

10_019

4_742

317 – 384

583 – 603

0

0

0

0,003

0,001

0

B443_B474

10_019

18

2

10_019

3_385

388 – 436

3

2

0,001

5

B86_B44

22_012

8

1

10_310

1_504

59 – 191

503 – 639

0

4

 

4

B86_B44

22_012

8

0

22_012

 

8

 

8

B44_B45_B187

11_424/3_610/5

544/7_345

6

0

11_424/3_610/5_544/7_345

 

6

 

6

  1. Test sequences were created in silico by combining sequence regions of assignable HML-2 cDNA sequences, with the aim to construct recombination events between transcripts from corresponding HML-2 loci. Pairwise comparisons, using the in-house Bio-Python script Locus-Assigner, were then performed for test and reference sequences. Column 1 denotes the cDNA sequence name. Column 2: best matching HML-2 proviral locus according to pairwise sequence comparisons with Locus-Assigner. The numbers given here disregard the PCR primer binding regions, and therefore are, for HERV-KX sequences B262, B12 and 93, below the <18 nt differences-threshold initially set for HERV-KX (see text). Due to the lack of a HERV taxonomy, and for the sake of simplicity, HML-2 proviral loci have been numbered artificially in this paper, with the first number indicating chromosomal location of the locus, and the second number being a consecutive number without further connotation. Column 3: nucleotide differences to best match. Column 4: number of recombinations according to RECCO. Column 5: proviral loci involved in recombination(s). More than one locus is given when different loci displayed identical (dis)similarities. Column 6: regions where recombination(s) occured, with the 5' end of the RT-PCR product being defined as nucleotide +1. Column 7: nucleotide differences to individual HML-2 loci. Column 8: p-values of particular predicted recombinations. Column 9: nucleotide differences remaining after considering recombination(s) (see text).