Fig. 2.
Fig. 2. Identification of Jk transcript mutation in the Finnish Jknull variant. / (A) Partial sequence analysis of the Jk transcript isolated from a wt Jk donor and from Finnish Jknull variant, Jk(S291P), within exon 9. The 2 Jk transcripts differ by a single base substitution T871C (star) changing serine (S) to proline (P) at position 291 in the Jk polypeptide. The display of the sequence diagram is from the Alf-Express DNA sequencer. (B) Left, schematic representation of the Jk(S291P) DNA genotyping assay by PCR-RFLP using primers SP-9 and SP-10. Exon 9 carries 2 polymorphisms that create 2 Mnl I sites, the first at position 838 corresponds to theJK*A/JK*B polymorphism, and the second at position 871 corresponds to the JK*B (S291P) null allele. Right, the 81-bp PCR product encompassing the 2 polymorphisms was cleaved byMnl I into 69- and 12-bp fragments in the Jk(S291P) mutant. As expected, the products from Jk(a−b+), Jk(Δ6), and Jk(Δ7) samples were uncut, whereas the product from Jk(a+b−) was cut into 16- and 65-bp fragments. Only the upper part of the gel containing the higher fragments is shown. Single base substitution is located by a star and size of fragments (bp) are given on the right.

Identification of Jk transcript mutation in the Finnish Jknull variant.

(A) Partial sequence analysis of the Jk transcript isolated from a wt Jk donor and from Finnish Jknull variant, Jk(S291P), within exon 9. The 2 Jk transcripts differ by a single base substitution T871C (star) changing serine (S) to proline (P) at position 291 in the Jk polypeptide. The display of the sequence diagram is from the Alf-Express DNA sequencer. (B) Left, schematic representation of the Jk(S291P) DNA genotyping assay by PCR-RFLP using primers SP-9 and SP-10. Exon 9 carries 2 polymorphisms that create 2 Mnl I sites, the first at position 838 corresponds to theJK*A/JK*B polymorphism, and the second at position 871 corresponds to the JK*B (S291P) null allele. Right, the 81-bp PCR product encompassing the 2 polymorphisms was cleaved byMnl I into 69- and 12-bp fragments in the Jk(S291P) mutant. As expected, the products from Jk(a−b+), Jk(Δ6), and Jk(Δ7) samples were uncut, whereas the product from Jk(a+b−) was cut into 16- and 65-bp fragments. Only the upper part of the gel containing the higher fragments is shown. Single base substitution is located by a star and size of fragments (bp) are given on the right.

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