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赖氨酰羟化酶基因中七个外显子的重复与该基因内一种重复序列的较长形式相关,是埃勒斯-当洛综合征VI型变体的常见病因。

Duplication of seven exons in the lysyl hydroxylase gene is associated with longer forms of a repetitive sequence within the gene and is a common cause for the type VI variant of Ehlers-Danlos syndrome.

作者信息

Heikkinen J, Toppinen T, Yeowell H, Krieg T, Steinmann B, Kivirikko K I, Myllylä R

机构信息

Biocenter and Department of Biochemistry, University of Oulu, Finland.

出版信息

Am J Hum Genet. 1997 Jan;60(1):48-56.

Abstract

The type VI variant of the Ehlers-Danlos syndrome (EDS) is a recessively inherited connective tissue disorder which, in most families, is due to a deficiency in lysyl hydroxylase activity. We have recently characterized a homozygous duplication of 8.9 kb in the lysyl hydroxylase gene (PLOD) in two EDS VI families. The duplication is caused by a homologous recombination of Alu sequences in introns 9 and 16. Using PCR, we have analyzed 26 additional EDS VI families from various countries and found that 7 of them have this duplication. Our data has shown a frequency of 19.1% for this mutant allele among 35 EDS VI families studied by us so far. Our haplotype analysis shows a variation in the sequence of DNA region surrounding the duplication. There is an association between a particular allele size class, the long form, at the dinucleotide repeat within intron 16 and the duplication mutation in PLOD. Screening of a general population revealed one positive finding among 582 alleles tested. An abnormal sequence in exon 17 of the gene, which generated a stop codon in the exon sequence and aberrant mRNA processing, was responsible for the nonfunctionality of the other allele in one of the compound heterozygous patients.

摘要

埃勒斯-当洛综合征(EDS)的VI型是一种隐性遗传的结缔组织疾病,在大多数家族中,是由于赖氨酰羟化酶活性缺乏所致。我们最近在两个EDS VI型家族中鉴定出赖氨酰羟化酶基因(PLOD)存在8.9 kb的纯合重复。该重复是由内含子9和16中的Alu序列同源重组引起的。我们使用聚合酶链反应(PCR)分析了来自不同国家的另外26个EDS VI型家族,发现其中7个家族存在这种重复。我们的数据显示,在我们迄今研究的35个EDS VI型家族中,该突变等位基因的频率为19.1%。我们的单倍型分析显示,重复周围DNA区域的序列存在变异。内含子16中二核苷酸重复处的特定等位基因大小类别(长形式)与PLOD中的重复突变之间存在关联。对普通人群的筛查显示,在检测的582个等位基因中发现1例阳性结果。该基因外显子17中的异常序列在外显子序列中产生了一个终止密码子并导致异常的信使核糖核酸(mRNA)加工,这是导致一名复合杂合子患者中另一个等位基因无功能的原因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d229/1712545/2accef4d1809/ajhg00001-0078-a.jpg

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