A Drosophila Model Reveals the Potential Role for mtt in Retinal Disease.
Wenfeng ChenWenmiao ZhongLingqi YuXiang LinJiayu XieZhenxing LiuPublished in: International journal of molecular sciences (2024)
Congenital stationary night blindness (CSNB) is a genetically heterogeneous inherited retinal disorder, caused by over 300 mutations in 17 different genes. While there are numerous fly models available for simulating ocular diseases, most are focused on mimicking retinitis pigmentosa (RP), with animal models specifically addressing CSNB limited to mammals. Here, we present a CSNB fly model associated with the mtt gene, utilizing RNA interference (RNAi) to silence the mtt gene in fly eyes (homologous to the mammalian GRM6 gene) and construct a CSNB model. Through this approach, we observed significant defects in the eye structure and function upon reducing mtt expression in fly eyes. This manifested as disruptions in the compound eye lens structure and reduced sensitivity to light responses. These results suggest a critical role for mtt in the function of fly adult eyes. Interestingly, we found that the mtt gene is not expressed in the photoreceptor neurons of adult flies but is localized to the inner lamina neurons. In summary, these results underscore the crucial involvement of mtt in fly retinal function, providing a framework for understanding the pathogenic mechanisms of CSNB and facilitating research into potential therapeutic interventions.
Keyphrases
- optical coherence tomography
- genome wide
- drosophila melanogaster
- genome wide identification
- copy number
- diabetic retinopathy
- optic nerve
- spinal cord
- dna methylation
- poor prognosis
- gene expression
- dna damage
- physical activity
- spinal cord injury
- genome wide analysis
- cataract surgery
- depressive symptoms
- dna repair
- mass spectrometry
- long non coding rna
- nucleic acid
- bioinformatics analysis