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Departments of Structural Biology and Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305
HLA class I alleles containing premature
termination codons (PTCs) are increasingly being found. To understand
their effects on MHC class I expression, HLA-A*2402
mutants containing PTCs were transfected into class I-deficient cells,
and expression of HLA-A mRNA and protein was determined.
In exons 2, 3, and 4, and in the 5' part of exon 5, PTCs reduced mRNA
levels by up to 90%, whereas in the 3' part of exon 5 and in exons 6
and 7 they had little effect. Transition in the extent of
nonsense-mediated mRNA decay occurred within a 48-nt segment of exon 5,
placed 58 nt upstream from the exon 5/exon 6 junction. This transition
did not conform to the positional rule obeyed by other genes, which
predicted it to be
5055 nt upstream of the exon 7/exon 8 junction
and thus placing it in exon 6. Mutants containing extra gene segments
showed the difference is caused by the small size of exons 5 and 6,
which renders them invisible to the surveillance machinery. For the
protein, a transition from secretion to membrane association occurs
within a 26-nt segment of exon 5, 17 nt upstream of the exon 5/exon 6
junction. Premature termination in exon 5 can produce secreted and
membrane-associated HLA-A variants expressed at high
levels.
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