TY - JOUR
T1 - Sequence polymorphisms in the apo(a) gene associated with specific levels of Lp(a) in plasma
AU - Mooser, Vincent
AU - Mancini, Francesco P.
AU - Bopp, Sabina
AU - Pethö-schramm, Attila
AU - Guerra, Rudy
AU - Boerwinkle, Eric
AU - Müller, Hans Joachim
AU - Hobbs, Helen H.
N1 - Funding Information:
We wish to thank Kathy Schueler and Tommy Hyatt for their excellent technical assistance and Jonathan Cohen, Michael Brown and David Russell for helpful discussions and review of the manuscript. We also want to thank Drs Santica Marcovinia and John Albers for measuring the plasma Lp(a) levels. This work was supported by NIH HL-47619, HL-20948, the Perot Family Fund, the Swiss Academy for Medical Sciences, the Ciba-Geigy Foundation and the Holderbank Foundation. Helen H.Hobbs is an Established Investigator of the American Heart Association.
PY - 1995/2
Y1 - 1995/2
N2 - Most of the Interindividual variations in plasma levels of lipoprotein(a) [Lp(a)] can be attributed to sequence differences linked to the apolipoprotein(a) [apo(a)] locus. Plasma levels of Lp(a) tend to be Inversely related to the number of kringle 4 (K4)-encoding sequences in the apo(a) gene, but there are several exceptions to this general trend. Other aspects of the apo(a) gene, In addition to the number of K4 repeats, affect plasma levels of Lp(a). To Identify sequences in the apo(a) gene that contribute to plasma Lp(a) levels, we characterized the relationship between a length polymorphism [(TTTTA)n] located 1·3 kb 5' of the first exon of the apo(a) gene, the number of K4 repeats in the gene, and the plasma levels of Lp(a). There was significant linkage disequilibrium between the number of TTTTA repeats and the number of K4 repeats. All of the apo(a) alleles with 11 TTTTA repeats contained fewer than 24 K4 repeats and were paradoxically associated with low plasma Lp(a) levels (<3 mg/dl). To determine whether this association was due to the effect of the 11 TTTTA copies on apo(a) gene transcription, we measured the ability of fragments containing 11 or eight TTTTA repeats to promote transcription when introduced into cultured human hepatocarcinoma cells. No difference was found in the transcriptional activity of the two fragments. The TTTTA repeat constitutes the first sequence polymorphism at the apo(a) locus, other than the number of K4 repeats, which is associated with plasma concentrations of Lp(a).
AB - Most of the Interindividual variations in plasma levels of lipoprotein(a) [Lp(a)] can be attributed to sequence differences linked to the apolipoprotein(a) [apo(a)] locus. Plasma levels of Lp(a) tend to be Inversely related to the number of kringle 4 (K4)-encoding sequences in the apo(a) gene, but there are several exceptions to this general trend. Other aspects of the apo(a) gene, In addition to the number of K4 repeats, affect plasma levels of Lp(a). To Identify sequences in the apo(a) gene that contribute to plasma Lp(a) levels, we characterized the relationship between a length polymorphism [(TTTTA)n] located 1·3 kb 5' of the first exon of the apo(a) gene, the number of K4 repeats in the gene, and the plasma levels of Lp(a). There was significant linkage disequilibrium between the number of TTTTA repeats and the number of K4 repeats. All of the apo(a) alleles with 11 TTTTA repeats contained fewer than 24 K4 repeats and were paradoxically associated with low plasma Lp(a) levels (<3 mg/dl). To determine whether this association was due to the effect of the 11 TTTTA copies on apo(a) gene transcription, we measured the ability of fragments containing 11 or eight TTTTA repeats to promote transcription when introduced into cultured human hepatocarcinoma cells. No difference was found in the transcriptional activity of the two fragments. The TTTTA repeat constitutes the first sequence polymorphism at the apo(a) locus, other than the number of K4 repeats, which is associated with plasma concentrations of Lp(a).
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U2 - 10.1093/hmg/4.2.173
DO - 10.1093/hmg/4.2.173
M3 - Article
C2 - 7757064
AN - SCOPUS:0028920022
SN - 0964-6906
VL - 4
SP - 173
EP - 181
JO - Human Molecular Genetics
JF - Human Molecular Genetics
IS - 2
ER -