Liu Melissa M, Farkas Michael, Spinnhirny Perrine, Pevet Paul, Pierce Eric, Hicks David, Zack Donald J
Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
Department of Ophthalmology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, United States of America.
PLoS One. 2017 Jul 31;12(7):e0179061. doi: 10.1371/journal.pone.0179061. eCollection 2017.
Cone photoreceptors are required for color vision and high acuity vision, and they die in a variety of retinal degenerations, leading to irreversible vision loss and reduced quality of life. To date, there are no approved therapies that promote the health and survival of cones. The development of novel treatments targeting cones has been challenging and impeded, in part, by the limitations inherent in using common rodent model organisms, which are nocturnal and rod-dominant, to study cone biology. The African Nile grass rat (Arvicanthis ansorgei), a diurnal animal whose photoreceptor population is more than 30% cones, offers significant potential as a model organism for the study of cone development, biology, and degeneration. However, a significant limitation in using the A. ansorgei retina for molecular studies is that A. ansorgei does not have a sequenced genome or transcriptome. Here we present the first de novo assembled and functionally annotated transcriptome for A. ansorgei. We performed RNA sequencing for A. ansorgei whole retina to a depth of 321 million pairs of reads and assembled 400,584 Trinity transcripts. Transcriptome-wide analyses and annotations suggest that our data set confers nearly full length coverage for the majority of retinal transcripts. Our high quality annotated transcriptome is publicly available, and we hope it will facilitate wider usage of A. ansorgei as a model organism for molecular studies of cone biology and retinal degeneration.
视锥光感受器对于色觉和高敏锐度视觉至关重要,并且它们会在多种视网膜变性中死亡,导致不可逆转的视力丧失和生活质量下降。迄今为止,尚无经批准的促进视锥细胞健康和存活的疗法。开发针对视锥细胞的新型治疗方法具有挑战性且受到阻碍,部分原因在于使用常见的啮齿动物模型生物(它们是夜行性且以视杆细胞为主)来研究视锥细胞生物学存在固有的局限性。非洲尼罗草鼠(Arvicanthis ansorgei)是一种昼行性动物,其光感受器群体中视锥细胞占比超过30%,作为研究视锥细胞发育、生物学和变性的模型生物具有巨大潜力。然而,将尼罗草鼠视网膜用于分子研究的一个重大限制是尼罗草鼠没有已测序的基因组或转录组。在此,我们展示了尼罗草鼠的首个从头组装且功能注释的转录组。我们对尼罗草鼠全视网膜进行了RNA测序,测序深度达到3.21亿对读数,并组装了400,584个Trinity转录本。全转录组分析和注释表明,我们的数据集几乎覆盖了大多数视网膜转录本的全长。我们高质量注释的转录组已公开可用,我们希望它将促进尼罗草鼠作为视锥细胞生物学和视网膜变性分子研究的模型生物得到更广泛的应用。