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1p32 处婴儿神经元蜡样脂褐质沉积症(INCL,CLN1)基因座的精细定位:多点分析中连锁不平衡的纳入。

Refined assignment of the infantile neuronal ceroid lipofuscinosis (INCL, CLN1) locus at 1p32: incorporation of linkage disequilibrium in multipoint analysis.

作者信息

Hellsten E, Vesa J, Speer M C, Mäkelä T P, Järvelä I, Alitalo K, Ott J, Peltonen L

机构信息

Department of Human Molecular Genetics, National Public Health Institute, Helsinki, Finland.

出版信息

Genomics. 1993 Jun;16(3):720-5. doi: 10.1006/geno.1993.1253.

Abstract

Infantile neuronal ceroid lipofuscinosis, INCL, CLN1, is an autosomally inherited progressive neurogenerative disorder. The disease results in the massive death of cortical neurons, suggesting an essential role for the CLN1 gene product in the normal neuronal maturation during the first years of life. Identification of new multiallelic markers has now made possible the construction of a refined genetic map encompassing the CLN1 locus at 1p32. Strong allelic association was detected with a new, highly polymorphic HY-TM1 marker. We incorporated this observed linkage disequilibrium into multipoint linkage analysis, which significantly increased the informativeness of the limited family material and facilitated refined assignment of the CLN1 locus.

摘要

婴儿神经元蜡样脂褐质沉积症(INCL,CLN1)是一种常染色体隐性遗传的进行性神经退行性疾病。该疾病导致皮质神经元大量死亡,这表明CLN1基因产物在生命最初几年的正常神经元成熟过程中起着至关重要的作用。新的多等位基因标记的鉴定使得构建一个精细的遗传图谱成为可能,该图谱涵盖了位于1p32的CLN1基因座。通过一个新的、高度多态的HY-TM1标记检测到了强等位基因关联。我们将观察到的这种连锁不平衡纳入多点连锁分析,这显著增加了有限家系材料的信息量,并有助于对CLN1基因座进行精细定位。

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