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本文引用的文献

1
Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.母源单亲二体性 6 号染色体导致视锥细胞功能障碍,揭示 TULP1 突变是其新的致病原因。
Ophthalmology. 2013 Jun;120(6):1239-46. doi: 10.1016/j.ophtha.2012.12.005. Epub 2013 Mar 15.
2
Non-syndromic retinal ciliopathies: translating gene discovery into therapy.非综合征性视网膜纤毛病:将基因发现转化为治疗方法。
Hum Mol Genet. 2012 Oct 15;21(R1):R111-24. doi: 10.1093/hmg/dds298. Epub 2012 Jul 26.
3
Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement.C8orf37 基因突变与常染色体隐性遗传的视网膜营养不良有关,这些疾病早期就会累及黄斑。
Am J Hum Genet. 2012 Jan 13;90(1):102-9. doi: 10.1016/j.ajhg.2011.11.015. Epub 2011 Dec 15.
4
XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription.XX 卵巢发育不全是由 PSMC3IP/HOP2 突变引起的,该突变会使雌激素驱动的转录共激活作用丧失。
Am J Hum Genet. 2011 Oct 7;89(4):572-9. doi: 10.1016/j.ajhg.2011.09.006. Epub 2011 Sep 29.
5
Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa.外显子组测序和顺式调控区作图鉴定出编码纤毛长度调节因子的 MAK 基因突变是导致色素性视网膜炎的原因之一。
Am J Hum Genet. 2011 Aug 12;89(2):253-64. doi: 10.1016/j.ajhg.2011.07.005.
6
The ciliopathy-associated protein homologs RPGRIP1 and RPGRIP1L are linked to cilium integrity through interaction with Nek4 serine/threonine kinase.纤毛病相关蛋白同源物 RPGRIP1 和 RPGRIP1L 通过与丝氨酸/苏氨酸激酶 Nek4 的相互作用与纤毛完整性相关联。
Hum Mol Genet. 2011 Sep 15;20(18):3592-605. doi: 10.1093/hmg/ddr280. Epub 2011 Jun 17.
7
MASP1 mutations in patients with facial, umbilical, coccygeal, and auditory findings of Carnevale, Malpuech, OSA, and Michels syndromes.Carnevale、Malpuech、OSA 和 Michels 综合征患者的面部、脐部、尾骨和耳部表现的 MASP1 突变。
Am J Hum Genet. 2010 Nov 12;87(5):679-86. doi: 10.1016/j.ajhg.2010.09.018. Epub 2010 Oct 28.
8
Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.外显子组测序鉴定出与 Sensénbrenner 综合征相关的 WDR35 变异。
Am J Hum Genet. 2010 Sep 10;87(3):418-23. doi: 10.1016/j.ajhg.2010.08.004.
9
Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.全外显子测序和纯合子作图确定细胞极性蛋白 GPSM2 中的突变是常染色体隐性遗传性耳聋 DFNB82 的致病原因。
Am J Hum Genet. 2010 Jul 9;87(1):90-4. doi: 10.1016/j.ajhg.2010.05.010. Epub 2010 Jun 17.
10
Rab and actomyosin-dependent fission of transport vesicles at the Golgi complex.Rab 和肌球蛋白依赖性运输小泡在高尔基体复合体中的分裂。
Nat Cell Biol. 2010 Jul;12(7):645-54. doi: 10.1038/ncb2067. Epub 2010 Jun 20.

RAB28 基因突变与常染色体隐性遗传的圆锥体-杆体细胞营养不良有关,该基因编码一种法尼基化的小 GTP 酶。

Mutations in RAB28, encoding a farnesylated small GTPase, are associated with autosomal-recessive cone-rod dystrophy.

机构信息

Department of Human Genetics, Radboud University Medical Centre, 6500 HB Nijmegen, the Netherlands.

出版信息

Am J Hum Genet. 2013 Jul 11;93(1):110-7. doi: 10.1016/j.ajhg.2013.05.005. Epub 2013 Jun 6.

DOI:10.1016/j.ajhg.2013.05.005
PMID:23746546
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3710761/
Abstract

The majority of the genetic causes of autosomal-recessive (ar) cone-rod dystrophy (CRD) are currently unknown. A combined approach of homozygosity mapping and exome sequencing revealed a homozygous nonsense mutation (c.565C>T [p.Glu189*]) in RAB28 in a German family with three siblings with arCRD. Another homozygous nonsense mutation (c.409C>T [p.Arg137*]) was identified in a family of Moroccan Jewish descent with two siblings affected by arCRD. All five affected individuals presented with hyperpigmentation in the macula, progressive loss of the visual acuity, atrophy of the retinal pigment epithelium, and severely reduced cone and rod responses on the electroretinogram. RAB28 encodes a member of the Rab subfamily of the RAS-related small GTPases. Alternative RNA splicing yields three predicted protein isoforms with alternative C-termini, which are all truncated by the nonsense mutations identified in the arCRD families in this report. Opposed to other Rab GTPases that are generally geranylgeranylated, RAB28 is predicted to be farnesylated. Staining of rat retina showed localization of RAB28 to the basal body and the ciliary rootlet of the photoreceptors. Analogous to the function of other RAB family members, RAB28 might be involved in ciliary transport in photoreceptor cells. This study reveals a crucial role for RAB28 in photoreceptor function and suggests that mutations in other Rab proteins may also be associated with retinal dystrophies.

摘要

常染色体隐性(ar)型 Cone-Rod 营养不良(CRD)的大多数遗传病因目前尚不清楚。采用纯合子作图和外显子组测序的联合方法,在一个有三个兄弟姐妹患有 arCRD 的德国家庭中发现 RAB28 存在纯合无义突变(c.565C>T [p.Glu189*])。在一个摩洛哥裔犹太人家庭中,另一个兄弟姐妹患有 arCRD,该家庭中发现了另一个纯合无义突变(c.409C>T [p.Arg137*])。所有五名受影响的个体均表现为黄斑区色素沉着、视力逐渐丧失、视网膜色素上皮萎缩以及视网膜电图上的锥体细胞和杆体细胞反应严重降低。RAB28 编码 Ras 相关的小 GTP 酶 Rab 亚家族的成员。选择性 RNA 剪接产生三种具有不同 C 末端的预测蛋白异构体,这些异构体均被本报告中 arCRD 家族中发现的无义突变截断。与通常被 geranylgeranylated 的其他 Rab GTPases 相反,RAB28 预计被 farnesylated。对大鼠视网膜的染色显示 RAB28 定位于视细胞的基底体和睫状根。类似于其他 RAB 家族成员的功能,RAB28 可能参与视细胞的纤毛运输。本研究揭示了 RAB28 在光感受器功能中的关键作用,并表明其他 Rab 蛋白的突变也可能与视网膜营养不良有关。