North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13

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• 作者：Kent W. Small ; MD¹ ; Adam P. DeLuca ; PhD² ; S. Scott Whitmore ; PhD² ; Thomas Rosenberg ; MD³ ; Rosemary Silva-Garcia ; MD¹ ; Nitin Udar ; PhD¹ ; Bernard Puech ; MD⁴ ; Charles A. Garcia ; MD⁵ ; Thomas A. Rice ; MD⁶ ; Gerald A. Fishman ; MD⁷ ; Elise H&eacute ; on ; MD⁸ ; James C. Folk ; MD² ; Luan M. Streb ; BA² ; Christine M. Haas ; BA² ; Luke A. Wiley ; PhD² ; Todd E. Scheetz ; PhD² ; John H. Fingert ; MD ; PhD² ; Robert F. Mullins ; PhD² ; Budd A. Tucker ; PhD² ; Edwin M. Stone ; MD ; PhD² ; ^{edwin-stone@uiowa.edu" class="auth_mail" title="E-mail the corresponding author}
• 关键词：AMD ; age-related macular degeneration ; bp ; base pairs ; DHS ; DNase 1 hypersensitivity site ; iPSC ; induced pluripotent stem cell ; NCMD ; North Carolina macular dystrophy ; 3D ; 3-dimensional
• 刊名：Ophthalmology
• 出版年：2016
• 出版时间：January 2016
• 年：2016
• 卷：123
• 期：1
• 页码：9-18
• 全文大小：3165 K

文摘

To identify specific mutations causing North Carolina macular dystrophy (NCMD).

Design

Whole-genome sequencing coupled with reverse transcription polymerase chain reaction (RT-PCR) analysis of gene expression in human retinal cells.

Participants

A total of 141 members of 12 families with NCMD and 261 unrelated control individuals.

Methods

Genome sequencing was performed on 8 affected individuals from 3 families affected with chromosome 6–linked NCMD (MCDR1) and 2 individuals affected with chromosome 5–linked NCMD (MCDR3). Variants observed in the MCDR1 locus with frequencies <1% in published databases were confirmed using Sanger sequencing. Confirmed variants absent from all published databases were sought in 8 additional MCDR1 families and 261 controls. The RT-PCR analysis of selected genes was performed in stem cell–derived human retinal cells.

Main Outcome Measures

Co-segregation of rare genetic variants with disease phenotype.

Results

Five sequenced individuals with MCDR1-linked NCMD shared a haplotype of 14 rare variants spanning 1 Mb of the disease-causing allele. One of these variants (V1) was absent from all published databases and all 261 controls, but was found in 5 additional NCMD kindreds. This variant lies in a DNase 1 hypersensitivity site (DHS) upstream of both the PRDM13 and CCNC genes. Sanger sequencing of 1 kb centered on V1 was performed in the remaining 4 NCMD probands, and 2 additional novel single nucleotide variants (V2 in 3 families and V3 in 1 family) were identified in the DHS within 134 bp of the location of V1. A complete duplication of the PRDM13 gene was also discovered in a single family (V4). The RT-PCR analysis of PRDM13 expression in developing retinal cells revealed marked developmental regulation. Next-generation sequencing of 2 individuals with MCDR3-linked NCMD revealed a 900-kb duplication that included the entire IRX1 gene (V5). The 5 mutations V1 to V5 segregated perfectly in the 102 affected and 39 unaffected members of the 12 NCMD families.

Conclusions

We identified 5 rare mutations, each capable of arresting human macular development. Four of these strongly implicate the involvement of PRDM13 in macular development, whereas the pathophysiologic mechanism of the fifth remains unknown but may involve the developmental dysregulation of IRX1.