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Targeted Resequencing and Analysis of the Diamond-Blackfan Anemia Disease Locus RPS19

Barrio, Alvaro Martinez (author)
Uppsala universitet,Centrum för bioinformatik,Bongcamp
Eriksson, Oskar (author)
Uppsala universitet,Medicinsk genetik,Institutionen för medicinska vetenskaper,Dahl
Badhai, Jitendra (author)
Uppsala universitet,Medicinsk genetik,Dahl
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Fröjmark, Anne-Sophie (author)
Uppsala universitet,Medicinsk genetik,Dahl
Bongcam-Rudloff, Erik (author)
Swedish University of Agricultural Sciences,Sveriges lantbruksuniversitet,Uppsala universitet,Centrum för bioinformatik,Institutionen för husdjursgenetik (HGEN),Department of Animal Breeding and Genetics,Uppsala University
Dahl, Niklas (author)
Uppsala universitet,Medicinsk genetik,Dahl
Schuster, Jens (author)
Uppsala universitet,Medicinsk genetik,Dahl
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 (creator_code:org_t)
 
2009-07-09
2009
English.
In: PLoS ONE. - : Public Library of Science (PLoS). - 1932-6203. ; 4:7, s. e6172-
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: The Ribosomal protein S19 gene locus (RPS19) has been linked to two kinds of red cell aplasia, Diamond-Blackfan Anemia (DBA) and Transient Erythroblastopenia in Childhood (TEC). Mutations in RPS19 coding sequences have been found in 25% of DBA patients, but not in TEC patients. It has been suggested that non-coding RPS19 sequence variants contribute to the considerable clinical variability in red cell aplasia. We therefore aimed at identifying non-coding variations associated with DBA or TEC phenotypes. METHODOLOGY/PRINCIPAL FINDINGS: We targeted a region of 19'980 bp encompassing the RPS19 gene in a cohort of 89 DBA and TEC patients for resequencing. We provide here a catalog of the considerable, previously unrecognized degree of variation in this region. We identified 73 variations (65 SNPs, 8 indels) that all are located outside of the RPS19 open reading frame, and of which 67.1% are classified as novel. We hypothesize that specific alleles in non-coding regions of RPS19 could alter the binding of regulatory proteins or transcription factors. Therefore, we carried out an extensive analysis to identify transcription factor binding sites (TFBS). A series of putative interaction sites coincide with detected variants. Sixteen of the corresponding transcription factors are of particular interest, as they are housekeeping genes or show a direct link to hematopoiesis, tumorigenesis or leukemia (e.g. GATA-1/2, PU.1, MZF-1). CONCLUSIONS: Specific alleles at predicted TFBSs may alter the expression of RPS19, modify an important interaction between transcription factors with overlapping TFBS or remove an important stimulus for hematopoiesis. We suggest that the detected interactions are of importance for hematopoiesis and could provide new insights into individual response to treatment.

Subject headings

LANTBRUKSVETENSKAPER  -- Veterinärmedicin (hsv//swe)
AGRICULTURAL SCIENCES  -- Veterinary Science (hsv//eng)
LANTBRUKSVETENSKAPER  -- Husdjursvetenskap (hsv//swe)
AGRICULTURAL SCIENCES  -- Animal and Dairy Sience (hsv//eng)

Keyword

MEDICINE
MEDICIN

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