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Insertion of Alu element responsible for acute intermittent porphyria
Author(s) -
Mustajoki Sami,
Ahola Helena,
Mustajoki Pertti,
Kauppinen Raili
Publication year - 1999
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1999)13:6<431::aid-humu2>3.0.co;2-y
Subject(s) - biology , acute intermittent porphyria , alu element , porphyria , genetics , element (criminal law) , computational biology , endocrinology , gene , genome , human genome , political science , law
In this study, we report a large Finnish family in which an Alu element interferes with the coding region of the porphobilinogen deaminase (PBGD) gene resulting in acute intermittent porphyria (AIP). Polymerase chain reaction (PCR) and single‐strand conformation polymorphism (SSCP) analysis of exon 5 among patients showed an abnormal band around 350 bp apart from the normal bands. Subcloning and sequencing of the fragment revealed a 333‐bp Alu sequence that was directly inserted into exon 5 in antisense orientation. The junction sequences included a 13‐bp target site duplication. This Alu cassette belongs to a Ya5 subfamily, one of the youngest and currently most active Alu subfamilies in evolution. The Alu insertion resulted in a dramatically decreased steady‐state level of the allelic transcript, as this Alu sequence could not be demonstrated by direct sequencing of the amplified cDNA synthesized from total RNA extracted from the patients' lymphoblast cell lines. A stop codon present in the reading frame causes premature termination of PBGD synthesis. The predicted polypeptide contains 64 of the 361 amino acids of PBGD, followed by 13 amino acids that are not identical to the PBGD polypeptide. To further characterize the consequences of the insertion, the Alu sequence was inserted into exon 5 of the PBGD cDNA and expressed in the eukaryotic COS‐1 cell line. The mutated construct expressed no enzyme activity comparable to that of the wild‐type PBGD; furthermore, no mutant protein could be detected by Western blot analysis. Hum Mutat 13:431–438, 1999. © 1999 Wiley‐Liss, Inc.