Literature DB >> 2413485

A retrovirus-like element occurs between the 3' breakpoints of two large deletions in the human beta-globin gene cluster.

D L Mager, P S Henthorn.   

Abstract

We have identified a novel repetitive family in human DNA. One member of this family is found downstream of the beta-globin gene cluster between the 3' breakpoints of the deletions associated with Chinese G gamma + (A gamma delta beta)O thalassemia and HPFH-2. This repetitive element is approximately 6 kbp in length and includes terminal direct repeats of 415 bp. Numerous DNA sequence features of the direct repeats (LTRs) and their flanking regions indicate that the element is a retrovirus-like structure. The most striking of these features is the presence of a histidine tRNA binding site just 3' to the 5' LTR. Accordingly the element is named RTVL-H (retrovirus-like element-histidine). The LTRs of the RTVL-H element are not strongly homologous to the LTRs of any previously described mammalian retrovirus or retrovirus-like element. Copy number estimates suggest that there are approximately 1000 RTVL-H elements in the human genome. The element found 3' (greater than 60 kbp) to the beta-globin gene appears to be a stable part of the normal genome. This retrovirus-like element is brought close to the fetal gamma-globin locus by the Chinese thalassemia deletion but is deleted in HPFH-1 and HPFH-2.

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Year:  1985        PMID: 2413485

Source DB:  PubMed          Journal:  Prog Clin Biol Res        ISSN: 0361-7742


  1 in total

1.  South-Italy β°-thalassemia: a novel deletion not removing the γ-globin silencing element and with 3' breakpoint in a hsRTVL-H element, associated with β°-thalassemia and high levels of HbF.

Authors:  Maria De Angioletti; Vincenzo Sabato; Gennaro Musollino; Romeo Prezioso; Clementina Carestia; Giuseppina Lacerra
Journal:  Haematologica       Date:  2013-06-28       Impact factor: 9.941

  1 in total

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