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. 2012 Nov 7;7(11):e49341. doi: 10.1371/journal.pone.0049341

Table 3. Chromosomal localization and relative cloning frequencies of cDNAs derived from transcribed HERV-E4-1 loci in malignant and non-malignant tissue of patient no. 2.

Transcript1 Location of amplicon(proviral locus)2 Chrom. localization cloning frequency in non-malignant tissue (%) cloning frequency in malignant tissue (%) Proximity to genes (<100 kb distance) found in tissue,reference
HERV-Ec1 chr1∶185155301–185155383 1q31.1 29% 7% PLA2G4A, withinintron 7
HERV-Ec6 (ERVE-4) chr6∶89432125–89432208 6q15 36% 20% RNGTT, withinintron 14 thalamus (Genbank; AK125006)
HERV-Ec7 chr7∶97420616–97420698 7q21.3 14% 40% ASNA (5′, 81 kb) OCM2 (3′, 31 kb)
HERV-Ec8 (ERVE-3) chr8∶8070254–8070336 or chr8∶12392139–123922213 8p23.1 or8p23.1 14% 0% leukemic cells (Prusty et al. [58])
HERV-Ec11 chr11∶3456532–3456614 11p15.4 0% 7% ZNF195 (5′, 99 kb)
HERV-Ec13 chr13∶40349963–40350045 13q14.1 7% 26% SLC25A15 (5′, 68 kb) SUGT1L1 (3′, 34 kb)
100% (14)4 100% (15)4
1

aliases according to HUGO Gene Nomenclature Committee are in parentheses [90].

2

Chromosomal localization of MOP-PCR amplicons according to the hg18/March 2006 human reference genome sequence as given by the UCSC Genome Browser.

3

HERV-Ec8 was mapped within a duplicated genome region, with both HERV-Ec8 sequences displaying only 20 nt differences along 8 kb. Assignment to one or the other locus is therefore not possible due to high sequence similarity.

4

Total number of sequenced cDNA clones.

Abbreviations: no., number; chr, chromosome.