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A comprehensive system for consistent numbering of HCV sequences, proteins and epitopes

  • Carla Kuiken(corresponding author)
    ,
  • Christophe Combet
    ,
  • Jens Bukh
    ,
  • Tadasu Shin-I
    ,
  • Gilbert Deleage
    ,
  • Masashi Mizokami
*Corresponding author for this work
  • Los Alamos National Laboratory
    ,
  • Universite Claude Bernard Lyon 1
    ,
  • University of Copenhagen
    ,
  • National Institutes of Health
    ,
  • Nagoya City University
    ,
  • Innogenetics
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

This numbering proposal, using the AF009606 (isolate H77) sequence as a reference, should be able to unequivocally number all possible mutations in HCV, both natural and manmade. The HCV sequence databases8 and the Los Alamos HCV immunology database9 (as well as the Los Alamos HIV database) number positions and epitopes according to this system. Moreover, the databases websites provides tools for finding stretches of sequence by their numbers, for assigning start and end coordinates to a sequence, and for converting between the various numbering systems. Numbering HCV nucleotide sequences is done by analogy to H77. The first step is aligning your sequence to H77. If there is no length variation, the numbering is straightforward; nucleotide numbers run from 1 (start of 5′ UTR) to 9646 (end of 3′ UTR). Insertions relative to H77 are labeled with letters. Protein numbering works like the nucleotide numbering, but starts at the start of the polyprotein. The sequence databases will support both systems, but use polyprotein numbering as a basis. Absolute numbering moves across the coding regions, relative numbering starts over at every coding region. Relative numbering is almost exclusively used for proteins, polyprotein numbering mainly in immunology, protein numbering in drug resistance research. The Los Alamos immunology database uses polyprotein numbering. The 5′ UTR numbering starts at 1 and ends at 341; the Core cds starts at 342. The numbering of the 3′ UTR starts at 9378 (after the stop codon), but complications arise due to the variable length of the PPT. The UTR consists of 3 elements: a variable 5′ region, the PPT, and a conserved 3′ region, often called X. The first region is numbered 9378-9410. The PPT consists almost entirely of T's and therefore cannot be meaningfully aligned; it is numbered according to its length in H77, 9411-9545. The X region starts at 9546 (regardless of its actual location, which depends on the length of the PPT) and ends at 9646.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1355-1361 (7 pages)

Journal (Volume, Issue Number)

Hepatology (Volume 44, Issue 5)

Publication milestones

  • Published - 11/2006

Publication status

Published - 11/2006

ISSN

0270-9139

Publication IDs

  • Scopus: 33750999948
  • PubMed: 17058236

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
1.32
SciVal
Author count
21
SciVal
citations
86
SciVal
Paper percentile
93
SciVal
Top percentile
10
Fractional count
1
Fractional count
0.05
Fractional count
20
Fractional count
0.95
Fractional count
1
Fractional count
1

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Captures
71
Citation count
102