Ogando Diego G, Dahlquist Kam D, Alizadeh Mitra, Kunchithapautham Kannan, Li Jun, Yu Nicole, LaVail Matthew M, Rohrer Bärbel, Vollrath Douglas, Danciger Michael
Department of Biology, Loyola Marymount University, Los Angeles, CA 90045-2659, USA.
Mol Vis. 2010 Jun 5;16:1004-18.
In a previous study, several quantitative trait loci (QTL) that influence age-related degeneration (ageRD) were identified in a cross between the albino strains B6(Cg)-Tyr(c-2J)/J (B6a) and BALB/cByJ (C). The Chromosome (Chr) 6 and Chr 10 QTL were the strongest and most highly significant loci and both involved B6a protective alleles. The QTL were responsible for 21% and 9% of the variance in phenotypes, respectively. We focused on these two QTL to identify candidate genes.
DNA microarrays were used for the two mouse strains at four and eight months of age to identify genes that are differentially regulated and map to either QTL. Gene Ontology (GO) analysis of the differentially expressed genes was performed to identify possible processes and pathways associated with ageRD. To identify additional candidates, database analyses (Positional Medline or PosMed) were used. Based on differential expression, PosMed, and the presence of reported polymorphisms, five genes per QTL were selected for further study by sequencing analysis and qRT-PCR. Tumor necrosis factor, alpha- induced protein 3 (Tnfaip3; on a C57BL/6J (B6) background) was phenotypically tested. Single nucleotide polymorphisms (SNPs) flanking this gene were correlated with outer nuclear layer thickness (ONL), and eight-month-old Tnfaip3(+/-) mice were tested for ageRD.
Polymorphisms were found in the coding regions of eight genes. Changes in gene expression were identified by qRT-PCR for Hexokinase 2 (Hk2) and Docking protein 1 (Dok1) at four months and for Dok1 and Tnfaip3 at eight months. Tnfaip3 was selected for phenotypic testing due to differential expression and the presence of two nonsynonymous mutations. However, when ONL thickness was compared in eight-month-old congenic Tnfaip3(+/-) and Tnfaip3(+/+) mice, no differences were found, suggesting that Tnfaip3 is not the quantitative trait gene (QTG) for the Chr 10 QTL. The GO analysis revealed that GO terms associated with stress and cell remodeling are overrepresented in the ageRD-sensitive C strain compared with the B6a strain with age (eight months). In the ageRD-resistant B6a strain, compared with the C strain, GO terms associated with antioxidant response and the regulation of blood vessel size are overrepresented with age.
The analyses of differentially expressed genes and the PosMed database yielded candidate genes for the Chr 6 and Chr 10 QTL. HtrA serine peptidase 2 (Htra2), Dok1, and Tnfaip3 were deemed most promising because of their known roles in apoptosis and our finding of nonsynonymous substitutions between B6a and C strains. While Tnfaip3 was excluded as the QTG for the Chr 10 QTL, Dok1 and Htra2 remain good candidates for the Chr 6 QTL. Finally, the GO term analysis further supports the general hypothesis that oxidative stress is involved in ageRD.
在之前的一项研究中,在白化病品系B6(Cg)-Tyr(c-2J)/J(B6a)和BALB/cByJ(C)的杂交后代中鉴定出了几个影响年龄相关性退变(ageRD)的数量性状基因座(QTL)。6号染色体(Chr)和10号染色体的QTL是最强且最显著的基因座,两者都涉及B6a保护性等位基因。这些QTL分别导致表型变异的21%和9%。我们聚焦于这两个QTL来鉴定候选基因。
使用DNA微阵列对4月龄和8月龄的这两种小鼠品系进行分析,以鉴定差异表达且定位于任一QTL的基因。对差异表达基因进行基因本体论(GO)分析,以鉴定与ageRD相关的可能过程和途径。为了鉴定其他候选基因,使用了数据库分析(定位医学文献检索或PosMed)。基于差异表达、PosMed以及已报道的多态性,每个QTL选择5个基因通过测序分析和qRT-PCR进行进一步研究。对肿瘤坏死因子α诱导蛋白3(Tnfaip3;在C57BL/6J(B6)背景下)进行了表型测试。该基因侧翼的单核苷酸多态性(SNP)与外核层厚度(ONL)相关,并对8月龄的Tnfaip3(+/-)小鼠进行了ageRD测试。
在8个基因的编码区发现了多态性。通过qRT-PCR鉴定出4月龄时己糖激酶2(Hk2)和对接蛋白1(Dok1)以及8月龄时Dok1和Tnfaip3的基因表达变化。由于差异表达和存在两个非同义突变,选择Tnfaip3进行表型测试。然而,当比较8月龄同基因Tnfaip3(+/-)和Tnfaip3(+/+)小鼠的ONL厚度时,未发现差异,这表明Tnfaip3不是10号染色体QTL的数量性状基因(QTG)。GO分析显示,与应激和细胞重塑相关的GO术语在随年龄增长(8个月)的ageRD敏感C品系中比B6a品系中更丰富。在抗ageRD的B6a品系中,与C品系相比,与抗氧化反应和血管大小调节相关的GO术语随年龄增长更丰富。
差异表达基因分析和PosMed数据库分析产生了6号染色体和10号染色体QTL的候选基因。HtrA丝氨酸蛋白酶2(Htra2)、Dok1和Tnfaip3因其在细胞凋亡中的已知作用以及我们在B6a和C品系之间发现的非同义替换而被认为最有前景。虽然Tnfaip3被排除为10号染色体QTL的QTG,但Dok1和Htra2仍是6号染色体QTL的良好候选基因。最后,GO术语分析进一步支持了氧化应激参与ageRD的一般假设。