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位于脊髓性肌萎缩关键区域的D5S351和D5S1414在伊朗人群中代表了新的信息性标记。

D5S351 and D5S1414 located at the spinal muscular atrophy critical region represent novel informative markers in the Iranian population.

作者信息

Sedghi Maryam, Vallian Sadeq

机构信息

Division of Genetics, Department of Biology, Faculty of Science, University of Isfahan, Isfahan, Islamic Republic of Iran.

出版信息

Meta Gene. 2015 Nov 10;7:16-9. doi: 10.1016/j.mgene.2015.10.006. eCollection 2016 Feb.

Abstract

Spinal muscular atrophy (SMA) is a degenerative neuromuscular disease associated with progressive symmetric weakness and atrophy of the limb muscles. In view of the involvement of numerous point mutations and deletions associated with the disease, the application of polymorphic markers flanking the SMA critical region could be valuable in molecular diagnosis of the disease. In the present study, D5S351 and D5S1414 polymorphic markers located at the SMA critical region in the Iranian populations were characterized. Genotyping of the markers indicated the presence of six and nine different alleles for D5S351 and D5S1414, respectively. Haplotype frequency estimation in 25 trios families and 75 unrelated individuals indicated the presence of six informative haplotypes with frequency higher than 0.05 in the studied population. Furthermore, the D' coefficient and the χ(2) value for D5S351 and D5S1414 markers revealed the presence of linkage disequilibrium between the two markers in the Iranians. These data suggested that D5S351 and D5S1414 could be suggested as informative markers for linkage analysis and molecular diagnosis of SMA in the Iranian population.

摘要

脊髓性肌萎缩症(SMA)是一种退行性神经肌肉疾病,与肢体肌肉进行性对称性无力和萎缩相关。鉴于该疾病涉及众多点突变和缺失,位于SMA关键区域侧翼的多态性标记物在该疾病的分子诊断中可能具有重要价值。在本研究中,对位于伊朗人群SMA关键区域的D5S351和D5S1414多态性标记物进行了特征分析。这些标记物的基因分型表明,D5S351和D5S1414分别存在6种和9种不同的等位基因。对25个三联体家庭和75个无关个体的单倍型频率估计表明,在所研究的人群中存在6种信息性单倍型,其频率高于0.05。此外,D5S351和D5S1414标记物的D'系数和χ(2)值表明这两个标记物在伊朗人群中存在连锁不平衡。这些数据表明,D5S351和D5S1414可被建议作为伊朗人群中SMA连锁分析和分子诊断的信息性标记物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b5f/4660382/e4811a786fa6/gr1.jpg

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本文引用的文献

1
Molecular analysis of SMN1, SMN2, NAIP, GTF2H2, and H4F5 genes in 157 Chinese patients with spinal muscular atrophy.
Gene. 2013 Apr 15;518(2):325-9. doi: 10.1016/j.gene.2012.12.109. Epub 2013 Jan 23.
2
Newborn and carrier screening for spinal muscular atrophy.
Am J Med Genet A. 2010 Jul;152A(7):1608-16. doi: 10.1002/ajmg.a.33474.
3
Carrier frequency of SMA by quantitative analysis of the SMN1 deletion in the Iranian population.
Eur J Neurol. 2010 Jan;17(1):160-2. doi: 10.1111/j.1468-1331.2009.02693.x. Epub 2009 Jun 15.
4
Ramblings in the history of spinal muscular atrophy.
Neuromuscul Disord. 2009 Jan;19(1):69-73. doi: 10.1016/j.nmd.2008.10.004. Epub 2008 Oct 31.
5
Analysis of point mutations in the SMN1 gene in SMA patients bearing a single SMN1 copy.
Neuromuscul Disord. 2007 Jun;17(6):476-81. doi: 10.1016/j.nmd.2007.03.003. Epub 2007 May 1.
7
A comparison of phasing algorithms for trios and unrelated individuals.
Am J Hum Genet. 2006 Mar;78(3):437-50. doi: 10.1086/500808. Epub 2006 Jan 26.
8
2LD, GENECOUNTING and HAP: Computer programs for linkage disequilibrium analysis.
Bioinformatics. 2004 May 22;20(8):1325-6. doi: 10.1093/bioinformatics/bth071. Epub 2004 Feb 10.
9
Genetic risk assessment in carrier testing for spinal muscular atrophy.
Am J Med Genet. 2002 Jul 15;110(4):301-7. doi: 10.1002/ajmg.10425.

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