Local base order influences the origin of ccr5 deletions mediated by DNA slip replication.

Abstract:

:CCR5 is a seven-transmembrane G-protein-coupled receptor that binds the CC-chemokines including RANTES, eotaxin, MIP-1alpha and beta. CCR5 serves as an essential coreceptor for cell entry of R5 (macrophage-tropic, nonsyncytium-inducing) strains of HIV-1. To date, four deletions have been found in human and primate ccr5. There is little evidence, however, on how these deletion mutations occur. In the present study, we analyzed ccr5 sequences of both mutants and wild type and found that direct repeats flanked the breakpoints of the deletions, suggesting that these deletions resulted from slipped mispairing during DNA replication. Of particular interest was the location of these deletions in or near the regions with higher negative FORS-D values. High negative FORS-D values stand for high stem-loop potential determined by base order and influence mainly the formation of stem-loop structures. Therefore, the particular location of these deletions suggests that the local sequence of bases might be important in the initiation of deletions mediated by DNA slip replication in concert with direct repeats.

journal_name

Biochem Genet

journal_title

Biochemical genetics

authors

Zhang CY,Wei JF,Het SH

subject

Has Abstract

pub_date

2005-06-01 00:00:00

pages

229-37

issue

5-6

eissn

0006-2928

issn

1573-4927

journal_volume

43

pub_type

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