Onecut1 and Onecut2 play critical roles in the development of the mouse retina

PLoS ONE

Volumn 9, Issue 10, 2014, Pages

  Goetz, Jillian J ^a   Martin, Gregory M ^a,b   Chowdhury, Rebecca ^a   Trimarchi, Jeffrey M ^a  

^a IOWA STATE UNIVERSITY   (United States)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLIAL FIBRILLARY ACIDIC PROTEIN; HERMES ANTIGEN; MELANOPSIN; TRANSCRIPTION FACTOR LHX1; TRANSCRIPTION FACTOR LIM1; TRANSCRIPTION FACTOR MATH5; TRANSCRIPTION FACTOR ONECUT; TRANSCRIPTION FACTOR ONECUT1; TRANSCRIPTION FACTOR ONECUT2; TRANSCRIPTION FACTOR SOX4; TRANSCRIPTOME; UNCLASSIFIED DRUG; HEPATOCYTE NUCLEAR FACTOR 6; HOMEODOMAIN PROTEIN; ONECUT1 PROTEIN, MOUSE; ONECUT2 PROTEIN, MOUSE; TRANSCRIPTION FACTOR;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DEATH; CELL FATE; CONTROLLED STUDY; DOWN REGULATION; GENE EXPRESSION; GENOTYPE; MICROARRAY ANALYSIS; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PHOTORECEPTOR CELL; PROTEIN EXPRESSION; PROTEIN FUNCTION; RETINA AMACRINE CELL; RETINA CONE; RETINA DEGENERATION; RETINA DEVELOPMENT; RETINA GANGLION CELL; RETINA HORIZONTAL NERVE CELL; RNA ISOLATION; UPREGULATION; ANIMAL; CYTOLOGY; GENE EXPRESSION REGULATION; GROWTH, DEVELOPMENT AND AGING; KNOCKOUT MOUSE; METABOLISM; PHYSIOLOGY; RETINA;

ANIMALS; GENE EXPRESSION REGULATION; HEPATOCYTE NUCLEAR FACTOR 6; HOMEODOMAIN PROTEINS; MICE, KNOCKOUT; RETINA; RETINAL HORIZONTAL CELLS; TRANSCRIPTION FACTORS; TRANSCRIPTOME;

EID: 84908013298     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0110194     Document Type: Article

References (47)

1. Edlund T, Jessell TM (1999) Progression from extrinsic to intrinsic signaling in cell fate specification: a view from the nervous system. Cell 96: 211-224.
2. Goetz JJ, Farris C, Chowdhury R, Trimarchi JM (2014) Making of a Retinal Cell. International Review of Cell and Molecular Biology. Elsevier, Vol. 308. 273-321. Available: http://linkinghub.elsevier.com/retrieve/pii/B9780128000977000075. Accessed 12 May 2014.
3. He J, Zhang G, Almeida AD, Cayouette M, Simons BD, et al. (2012) How Variable Clones Build an Invariant Retina. Neuron 75: 786-798. doi:10.1016/j.neuron.2012.06.033.
4. Livesey FJ, Cepko CL (2001) Vertebrate neural cell-fate determination: lessons from the retina. Nat Rev Neurosci 2: 109-118. doi:10.1038/35053522.
5. Chen Z, Li X, Desplan C (2012) Deterministic or Stochastic Choices in Retinal Neuron Specification. Neuron 75: 739-742. doi:10.1016/j.neuron.2012.08.008.
6. Isshiki T, Pearson B, Holbrook S, Doe CQ (2001) Drosophila neuroblasts sequentially express transcription factors which specify the temporal identity of their neuronal progeny. Cell 106: 511-521.
7. Turner DL, Cepko CL (1987) A common progenitor for neurons and glia persists in rat retina late in development. Nature 328: 131-136. doi:10.1038/328131a0.
8. Turner DL, Snyder EY, Cepko CL (1990) Lineage-independent determination of cell type in the embryonic mouse retina. Neuron 4: 833-845.
9. Masland RH (2001) The fundamental plan of the retina. Nat Neurosci 4: 877-886. doi:10.1038/nn0901-877.
10. Cherry TJ, Trimarchi JM, Stadler MB, Cepko CL (2009) Development and diversification of retinal amacrine interneurons at single cell resolution. Proc Natl Acad Sci 106: 9495-9500. doi:10.1073/pnas.0903264106.
11. Sidman R (1961) Histogenesis of mouse retina studied with thymidine-H3. In: Smelser G, editor. The Structure of the Eye. New York: Academic Press. 487-506.
12. Voinescu PE, Kay JN, Sanes JR (2009) Birthdays of retinal amacrine cell subtypes are systematically related to their molecular identity and soma position. J Comp Neurol 517: 737-750. doi:10.1002/cne.22200.
13. Young RW (1985) Cell differentiation in the retina of the mouse. Anat Rec 212: 199-205. doi:10.1002/ar.1092120215.
14. Young RW (1985) Cell proliferation during postnatal development of the retina in the mouse. Dev Brain Res 21: 229-239. doi:10.1016/0165-3806(85)90211-1.
15. Cepko CL (1996) The patterning and onset of opsin expression in vertebrate retinae. Curr Opin Neurobiol 6: 542-546.
16. Trimarchi JM, Stadler MB, Cepko CL (2008) Individual Retinal Progenitor Cells Display Extensive Heterogeneity of Gene Expression. PLoS ONE 3: e1588. doi:10.1371/journal.pone.0001588.
17. Brzezinski JA 4th, Prasov L, Glaser T (2012) Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle. Dev Biol 365: 395-413. doi:10.1016/j.ydbio.2012.03.006.
18. Skowronska-Krawczyk D, Chiodini F, Ebeling M, Alliod C, Kundzewicz A, et al. (2009) Conserved regulatory sequences in Atoh7 mediate non-conserved regulatory responses in retina ontogenesis. Development 136: 3767-3777. doi:10.1242/dev.033449.
19. Feng L, Xie Z, Ding Q, Xie X, Libby RT, et al. (2010) MATH5 controls the acquisition of multiple retinal cell fates. Mol Brain 3: 36. doi:10.1186/1756-6606-3-36.
20. Yang Z, Ding K, Pan L, Deng M, Gan L (2003) Math5 determines the competence state of retinal ganglion cell progenitors. Dev Biol 264: 240-254. doi:10.1016/j.ydbio.2003.08.005.
21. Brown NL, Patel S, Brzezinski J, Glaser T (2001) Math5 is required for retinal ganglion cell and optic nerve formation. Dev Camb Engl 128: 2497-2508.
22. Kay JN, Finger-Baier KC, Roeser T, Staub W, Baier H (2001) Retinal Ganglion Cell Genesis Requires lakritz, a Zebrafish atonal Homolog. Neuron 30: 725-736. doi:10.1016/S0896-6273(01)00312-9.
23. Wang SW (2001) Requirement for math5 in the development of retinal ganglion cells. Genes Dev 15: 24-29. doi:10.1101/gad.855301.
24. Wu F, Sapkota D, Li R, Mu X (2012) Onecut 1 and Onecut 2 are potential regulators of mouse retinal development. J Comp Neurol 520: 952-969. doi:10.1002/cne.22741.
25. Clotman F, Lannoy VJ, Reber M, Cereghini S, Cassiman D, et al. (2002) The onecut transcription factor HNF6 is required for normal development of the biliary tract. Dev Camb Engl 129: 1819-1828.
26. Lemaigre FP, Durviaux SM, Truong O, Lannoy VJ, Hsuan JJ, et al. (1996) Hepatocyte nuclear factor 6, a transcription factor that contains a novel type of homeodomain and a single cut domain. Proc Natl Acad Sci U S A 93: 9460-9464.
27. Furuno K, Ikeda K, Hamano S, Fukuyama K, Sonoda M, et al. (2008) Onecut transcription factor OC2 is a direct target of T-bet in type-1 T-helper cells. Genes Immun 9: 302-308. doi:10.1038/gene.2008.18.
28. Jacquemin P, Lemaigre FP, Rousseau GG (2003) The Onecut transcription factor HNF-6 (OC-1) is required for timely specification of the pancreas and acts upstream of Pdx-1 in the specification cascade. Dev Biol 258: 105-116.
29. Wu F, Li R, Umino Y, Kaczynski TJ, Sapkota D, et al. (2013) Onecut1 Is Essential for Horizontal Cell Genesis and Retinal Integrity. J Neurosci 33: 13053-13065. doi:10.1523/JNEUROSCI.0116-13.2013.
30. Morrow EM, Chen C-MA, Cepko CL (2008) Temporal order of bipolar cell genesis in the neural retina. Neural Develop 3: 2. doi:10.1186/1749-8104-3-2.
31. Molday RS, MacKenzie D (1983) Monoclonal antibodies to rhodopsin: characterization, cross-reactivity, and application as structural probes. Biochemistry (Mosc) 22: 653-660. doi:10.1021/bi00272a020.
32. Blackshaw S, Harpavat S, Trimarchi J, Cai L, Huang H, et al. (2004) Genomic Analysis of Mouse Retinal Development. PLoS Biol 2: e247. doi:10.1371/journal.pbio.0020247.
33. Kim DS, Ross SE, Trimarchi JM, Aach J, Greenberg ME, et al. (2008) Identification of molecular markers of bipolar cells in the murine retina. J Comp Neurol 507: 1795-1810. doi:10.1002/cne.21639.
34. Poché RA, Kwan KM, Raven MA, Furuta Y, Reese BE, et al. (2007) Lim1 is essential for the correct laminar positioning of retinal horizontal cells. J Neurosci Off J Soc Neurosci 27: 14099-14107. doi:10.1523/JNEUROSCI.4046-07.2007.
35. Lewis GP, Fisher SK (2003) Up-regulation of glial fibrillary acidic protein in response to retinal injury: its potential role in glial remodeling and a comparison to vimentin expression. Int Rev Cytol 230: 263-290.
36. Rattner A (2005) The Genomic Response to Retinal Disease and Injury: Evidence for Endothelin Signaling from Photoreceptors to Glia. J Neurosci 25: 4540-4549. doi:10.1523/JNEUROSCI.0492-05.2005.
37. Samardzija M, Wariwoda H, Imsand C, Huber P, Heynen SR, et al. (2012) Activation of survival pathways in the degenerating retina of rd10 mice. Exp Eye Res 99: 17-26. doi:10.1016/j.exer.2012.04.004.
38. Swiderski RE, Nishimura DY, Mullins RF, Olvera MA, Ross JL, et al. (2007) Gene Expression Analysis of Photoreceptor Cell Loss in Bbs4-Knockout Mice Reveals an Early Stress Gene Response and Photoreceptor Cell Damage. Invest Ophthalmol Vis Sci 48: 3329-3340. doi:10.1167/iovs.06-1477.
39. Templeton JP, Freeman NE, Nickerson JM, Jablonski MM, Rex TS, et al. (2013) Innate Immune Network in the Retina Activated by Optic Nerve Crush. Invest Ophthalmol Vis Sci 54: 2599-2606. doi:10.1167/iovs.12-11175.
40. Chaitin MH, Ankrum MT, Wortham HS (1996) Distribution of CD44 in the retina during development and the rds degeneration. Brain Res Dev Brain Res 94: 92-98.
41. Grünert U, Wässle H (1993) Immunocytochemical localization of glycine receptors in the mammalian retina. J Comp Neurol 335: 523-537. doi:10.1002/cne.903350405.
42. Jiang Y, Ding Q, Xie X, Libby RT, Lefebvre V, et al. (2013) Transcription Factors SOX4 and SOX11 Function Redundantly to Regulate the Development of Mouse Retinal Ganglion Cells. J Biol Chem 288: 18429-18438. doi:10.1074/jbc.M113.478503.
43. Schmidt TM, Do MTH, Dacey D, Lucas R, Hattar S, et al. (2011) Melanopsin-Positive Intrinsically Photosensitive Retinal Ganglion Cells: From Form to Function. J Neurosci 31: 16094-16101. doi:10.1523/JNEUROSCI.4132-11.2011.
44. Jin Z, Zhang J, Klar A, Chédotal A, Rao Y, et al. (2003) Irx4-mediated regulation of Slit1 expression contributes to the definition of early axonal paths inside the retina. Dev Camb Engl 130: 1037-1048.
45. Trimarchi JM, Stadler MB, Roska B, Billings N, Sun B, et al. (2007) Molecular heterogeneity of developing retinal ganglion and amacrine cells revealed through single cell gene expression profiling. J Comp Neurol 502: 1047-1065. doi:10.1002/cne.21368.
46. Iyaguchi D, Yao M, Watanabe N, Nishihira J, Tanaka I (2007) DNA recognition mechanism of the ONECUT homeodomain of transcription factor HNF-6. Struct Lond Engl 1993 15: 75-83. doi:10.1016/j.str.2006.11.004.
47. Emerson MM, Surzenko N, Goetz JJ, Trimarchi J, Cepko CL (2013) Otx2 and Onecut1 Promote the Fates of Cone Photoreceptors and Horizontal Cells and Repress Rod Photoreceptors. Dev Cell 26: 59-72. doi:10.1016/j.devcel.2013.06.005.