The patterning of retinal horizontal cells: normalizing the regularity index enhances the detection of genomic linkage

Retinal neurons are often arranged as non-random distributions called “mosaics,” as their somata minimize proximity to neighboring cells of the same type. The horizontal cells serve as an example of such a mosaic, but little is known about the developmental mechanisms that underlie their patterning. To identify genes involved in this process, we have used three different spatial statistics to assess the patterning of the horizontal cell mosaic across a panel of genetically distinct recombinant inbred strains. To avoid the confounding effect of cell density, which varies twofold across these different strains, we computed the “real/random regularity ratio,” expressing the regularity of a mosaic relative to a randomly distributed simulation of similarly sized cells. To test whether this latter statistic better reflects the variation in biological processes that contribute to horizontal cell spacing, we subsequently compared the genomic linkage for each of these two traits, the regularity index, and the real/random regularity ratio, each computed from the distribution of nearest neighbor (NN) distances and from the Voronoi domain (VD) areas. Finally, we compared each of these analyses with another index of patterning, the packing factor. Variation in the regularity indexes, as well as their real/random regularity ratios, and the packing factor, mapped quantitative trait loci to the distal ends of Chromosomes 1 and 14. For the NN and VD analyses, we found that the degree of linkage was greater when using the real/random regularity ratio rather than the respective regularity index. Using informatic resources, we narrowed the list of prospective genes positioned at these two intervals to a small collection of six genes that warrant further investigation to determine their potential role in shaping the patterning of the horizontal cell mosaic.

[1]  Lucas Cheadle,et al.  The novel synaptogenic protein Farp1 links postsynaptic cytoskeletal dynamics and transsynaptic organization , 2012, The Journal of cell biology.

[2]  H. Wässle,et al.  The mosaic of nerve cells in the mammalian retina , 1978, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[3]  Stephen J Eglen,et al.  Development of regular cellular spacing in the retina: theoretical models. , 2006, Mathematical medicine and biology : a journal of the IMA.

[4]  Jeremy E. Cook,et al.  Spatial regularity among retinal neurons , 2003 .

[5]  B. Reese,et al.  Design principles and developmental mechanisms underlying retinal mosaics , 2015, Biological reviews of the Cambridge Philosophical Society.

[6]  R. W. Rodieck The density recovery profile: A method for the analysis of points in the plane applicable to retinal studies , 1991, Visual Neuroscience.

[7]  B. Reese,et al.  Mosaics of Islet-1-Expressing Amacrine Cells Assembled by Short-Range Cellular Interactions , 1997, The Journal of Neuroscience.

[8]  Robert W. Williams,et al.  Independent genomic control of neuronal number across retinal cell types. , 2014, Developmental cell.

[9]  Tiansen Li,et al.  Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells , 2007, Proceedings of the National Academy of Sciences.

[10]  B. Reese,et al.  Retinal horizontal cells: challenging paradigms of neural development and cancer biology , 2009, Development.

[11]  K. Yau,et al.  Guidance-Cue Control of Horizontal Cell Morphology, Lamination, and Synapse Formation in the Mammalian Outer Retina , 2012, The Journal of Neuroscience.

[12]  J. Cook,et al.  Spatial properties of retinal mosaics: An empirical evaluation of some existing measures , 1996, Visual Neuroscience.

[13]  H. Nakauchi,et al.  The role of Zic family zinc finger transcription factors in the proliferation and differentiation of retinal progenitor cells. , 2011, Biochemical and biophysical research communications.

[14]  M. A. Raven,et al.  Developmental improvement in the regularity and packing of mouse horizontal cells: Implications for mechanisms underlying mosaic pattern formation , 2005, Visual Neuroscience.

[15]  Robert W. Williams,et al.  Genetic modulation of horizontal cell number in the mouse retina , 2011, Proceedings of the National Academy of Sciences.

[16]  Lu Lu,et al.  Pituitary tumor-transforming gene 1 regulates the patterning of retinal mosaics , 2014, Proceedings of the National Academy of Sciences.

[17]  I. Hermans-Borgmeyer,et al.  Developmental expression of the estrogen receptor-related receptor γ in the nervous system during mouse embryogenesis , 2000, Mechanisms of Development.

[18]  M. A. Raven,et al.  Regularity and packing of the horizontal cell mosaic in different strains of mice , 2005, Visual Neuroscience.

[19]  Jack R. Davis,et al.  Identification of the mouse and rat orthologs of the gene mutated in Usher syndrome type IIA and the cellular source of USH2A mRNA in retina, a target tissue of the disease. , 2002, Genomics.

[20]  M. A. Raven,et al.  Somal positioning and dendritic growth of horizontal cells are regulated by interactions with homotypic neighbors , 2008, The European journal of neuroscience.

[21]  J. N. Kay,et al.  MEGF10 AND 11 MEDIATE HOMOTYPIC INTERACTIONS REQUIRED FOR MOSAIC SPACING OF RETINAL NEURONS , 2012, Nature.

[22]  M. A. Raven,et al.  Horizontal cell density and mosaic regularity in pigmented and albino mouse retina , 2002, The Journal of comparative neurology.

[23]  W. Stell,et al.  Cell-Type Specific Roles for PTEN in Establishing a Functional Retinal Architecture , 2012, PloS one.

[24]  S. Sockanathan,et al.  FARP1 Promotes the Dendritic Growth of Spinal Motor Neuron Subtypes through Transmembrane Semaphorin6A and PlexinA4 Signaling , 2009, Neuron.

[25]  R. Wong,et al.  Transient neurites of retinal horizontal cells exhibit columnar tiling via homotypic interactions , 2008, Nature Neuroscience.