Keller Sylvia, Prechtl Danielle, Aslanidis Charalampos, Ceglarek Uta, Thiery Joachim, Schmitz Gerd, Jahreis Gerhard
Friedrich Schiller University Jena, Institute of Nutrition, Jena, Germany.
Eur J Med Genet. 2011 Jul-Aug;54(4):e458-60. doi: 10.1016/j.ejmg.2011.05.003. Epub 2011 May 23.
Whilst conducting a scientific study, an elevated plasma plant sterol concentration of 3.07 mg/dL was established in one proband. Similar levels found in his mothers plasma (2.73 mg/dL) were suggestive of a heterozygous sitosterolemia. The resulting gene analysis for ATP binding cassette transporter G5/G8 (ABCG5/G8) revealed a heterozygous polymorphism in ABCG8 (Thr400Lys, rs4148217), which the proband had inherited from his father. However, a heterozygous amino acid exchange (Arg406Gln) in exon 9 of ABCG5 was revealed, which was inherited from his mother. Although not sufficient evidence exists to regard this sequence variation as a mutation, this previously unreleased sequence variation occurred in a "hot spot" area for sitosterolemia of the ABCG5 gene (exon 9) and the similar increased plasma plant sterol concentrations of the heterozygous mother contribute to the notion, that this very likely presents an inactivating mutation.
在进行一项科学研究时,一名先证者的血浆植物甾醇浓度升高至3.07mg/dL。在其母亲的血浆中发现了类似水平(2.73mg/dL),提示为杂合子谷甾醇血症。对ATP结合盒转运体G5/G8(ABCG5/G8)进行的基因分析显示,ABCG8存在杂合多态性(Thr400Lys,rs4148217),先证者从其父亲那里遗传了该多态性。然而,在ABCG5的外显子9中发现了一个杂合氨基酸交换(Arg406Gln),这是他从母亲那里遗传来的。尽管没有足够的证据将这种序列变异视为突变,但这种先前未报道的序列变异发生在ABCG5基因谷甾醇血症的“热点”区域(外显子9),并且杂合子母亲血浆植物甾醇浓度也有类似升高,这使得人们认为这很可能是一个失活突变。