THE IMPACT OF PARALOG GENES: DETECTION OF COPY NUMBER VARIATION IN SPINAL MUSCLE ATROPHY PATIENTS

Biocell

Sergio LAURITO¹ 

关键词: SMA;    CNV;    MLPA;    Paralog gene;   

DOI  :  

学科分类：仪器

来源: Biocell

【 摘 要 】

Spinal muscular atrophy (SMA) is caused by dysfunction of the alpha motor neurons of the spinal cord.It is an autosomal recessive disease associated to the SMN1 gene, located in the subtelomeric region of 5q13. Aparalog SMN2 gene is located at the centromeric region of the same chromosome, which apparently originated byan ancestral inverted duplication occurring only in humans. The exon sequence differs in two nucleotides in exon 7and exon 8, which leads to an SMN2 transcript that lacks exon 7 and results in a truncated protein. Part (10%) of theSMN2 transcripts avoids the splicing of exon 7 but most of the copies are dysfunctional. In a disease scenario, themore SMN2 copies the higher possibility to restore at least partly the effects of SMN1 deficiency. Some therapeuticapproaches are being developed to increase the expression of SMN2. To determine the number of SMN1 and SMN2copies, the methodology must distinguish accurately between both genes. In this work, we present the results obtainedusing multiplex ligation-dependent probe amplification (MLPA) in 60 SMA suspected patients/carriers derived fromdifferent regions of Argentina. In 32 of these DNA samples we found alterations in SMN1. Among these, 16 presented aheterozygous deletion (carrier status) and 14 an homozygous deletion (patient status) in exon 7 and 8 of SMN1. In onecase, exon 7 was found homozygously deleted but exon 8 presented a single copy, and in another case, exon 7 was foundheterozygously deleted while exon 8 was normal. Almost half of the patients (7/15) presented a normal diploid numberof SMN2 while the other half (8/15) presented an increased number. In this work we showed how a probe-basedmethodology such as MLPA was able to distinguish between the paralog genes and determine the amount of copies inDNA samples from suspected patients/carriers of SMA.

【 授权许可】

CC BY