RESUMEN
Ath1 is a quantitative trait locus on mouse chromosome 1 that renders C57BL/6 mice susceptible and C3H/He mice resistant to diet-induced atherosclerosis. The quantitative trait locus region encompasses 11 known genes, including Tnfsf4 (also called Ox40l or Cd134l), which encodes OX40 ligand. Here we report that mice with targeted mutations of Tnfsf4 had significantly (P Asunto(s)
Arteriosclerosis/genética
, Predisposición Genética a la Enfermedad
, Glicoproteínas de Membrana/fisiología
, Polimorfismo de Nucleótido Simple
, Sitios de Carácter Cuantitativo/genética
, Anciano
, Animales
, Aorta/metabolismo
, Aorta/patología
, Apolipoproteínas E/genética
, Apolipoproteínas E/fisiología
, Arteriosclerosis/metabolismo
, Arteriosclerosis/patología
, Estudios de Casos y Controles
, Colesterol en la Dieta
, Cruzamientos Genéticos
, Femenino
, Humanos
, Masculino
, Glicoproteínas de Membrana/genética
, Ratones
, Ratones Endogámicos BALB C
, Ratones Endogámicos C3H
, Ratones Endogámicos C57BL
, Ratones Noqueados
, Persona de Mediana Edad
, Ligando OX40
, Fenotipo
, Miembro 7 de la Superfamilia de Receptores de Factores de Necrosis Tumoral/fisiología
, Factores de Necrosis Tumoral
RESUMEN
The D allozyme of placental alkaline phosphatase (PLAP) displays enzymatic properties at variance with those of the common PLAP allozymes. We have deduced the amino acid sequence of the PLAP D allele by PCR cloning of its gene, ALPP. Two coding substitutions were found in comparison with the cDNA of the common PLAP F allele, i.e., 692C>G and 1352A>G, which translate into a P209R and E429G substitution. A single nucleotide primer extension (SNuPE) assay was developed using PCR primers that enable the amplification of a 1.9 kb PLAP fragment. Extension primers were then used on this PCR fragment to detect the 692C>G and 1352A>G substitution. The SNuPE assay on these two nucleotide substitutions enabled us to distinguish the PLAP F and D alleles from the PLAP S/I alleles. Functional studies on the D allozyme were made possible by constructing and expressing a PLAP D cDNA, i.e., [Arg209, Gly429]PLAP, into wild-type Chinese hamster ovary cells. We determined the k(cat) and K(m), of the PLAP S, F, and D allozymes using the non-physiological substrate p-nitrophenylphosphate at an optimal pH (9.8) as well as two physiological substrates, i.e., pyridoxal-5-phosphate and inorganic pyrophosphate at physiological pH (7.5). We found that the biochemical properties of the D allozyme of PLAP are significantly different from those of the common PLAP allozymes. These biochemical findings suggest that a suboptimal enzymatic function by the PLAP D allozyme may be the basis for the apparent negative selective pressure of the PLAP D allele. The development of the SNuPE assay will enable us to test the hypothesis that the PLAP D allele is subjected to intrauterine selection by examining genomic DNA from statistically informative population samples.