The expression of αA- and βB1-crystallin during normal development and regeneration, and proteomic analysis for the regenerating lens in Xenopus laevis

Molecular Vision

Volumn 17, Issue , 2011, Pages 768-778

  Zhao, Yongqing ^a   Ju, Furong ^a   Zhao, Yuanlin ^a   Wang, Lei ^a   Sun, Zhenglong ^a   Liu, Mingxin ^b   Gao, Lan ^a  

^a LANZHOU UNIVERSITY   (China)

^b TSINGHUA UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA CRYSTALLIN; BETA B1 CRYSTALLIN; BETA CRYSTALLIN; MESSENGER RNA; UNCLASSIFIED DRUG;

ARTICLE; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; EYE DEVELOPMENT; FUNCTIONAL PROTEOMICS; GENE EXPRESSION; IMMUNOFLUORESCENCE TEST; LENS; NONHUMAN; NUCLEOTIDE SEQUENCE; ONTOGENY; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN LOCALIZATION; REAL TIME POLYMERASE CHAIN REACTION; TWO DIMENSIONAL GEL ELECTROPHORESIS; XENOPUS LAEVIS;

ALPHA-CRYSTALLIN A CHAIN; ANIMALS; BETA-CRYSTALLIN B CHAIN; CLONING, MOLECULAR; ECTODERM; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; EMBRYO, NONMAMMALIAN; EMBRYONIC DEVELOPMENT; ESCHERICHIA COLI; GENE EXPRESSION REGULATION, DEVELOPMENTAL; IN SITU HYBRIDIZATION; LENS, CRYSTALLINE; POLYMERASE CHAIN REACTION; PROTEOMICS; RECOMBINANT PROTEINS; REGENERATION; RNA, MESSENGER; XENOPUS LAEVIS;

EID: 79955573035     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

References (51)

1. Stocum DL. Regenerative biology and medicine. J Musculoskelet Neuronal Interact 2002; 2:270-273. [PMID: 15758451]
2. Tsonis PA, Madhavan M, Tancous EE, Del Rio-Tsonis K. A newt's eye view of lens regeneration. Int J Dev Biol 2004; 48:975-980. [PMID: 15558488]
3. Tsonis PA, Del Rio-Tsonis K. Lens and retina regeneration: transdifferentiation, stem cells and clinical applications. Exp Eye Res 2004; 78:161-172. [PMID: 14729349]
4. Brockes JP, Kumar A. Plasticity and reprogramming of differentiated cells in amphibian regeneration. Nat Rev Mol Cell Biol 2002; 3:566-574. [PMID: 12154368]
5. Straube WL, Tanaka EM. Reversibility of the differentiated state: regeneration in amphibians. Artif Organs 2006; 30:743-755. [PMID: 17026573]
6. Chaar ZY, Tsilfidis C. Newt opportunities for understanding the dedifferentiation process. Scientific World Journal 2006; 6:55-64. [PMID: 17205187]
7. Stone LS. The Regeneration of the Crystalline Lens. Invest Ophthalmol 1965; 4:420-432. [PMID: 14340159]
8. Freeman G. Lens regeneration from the cornea in Xenopus laevis. J Exp Zool 1963; 154:39-65. [PMID: 14066571]
9. Bosco L. Transdifferentiation of ocular tissues in larval Xenopus laevis. Differentiation 1988; 39:4-15. [PMID: 3073094]
10. Filoni S, Bernardini S, Cannata SM. Experimental analysis of lens-forming capacity in Xenopus borealis larvae. J Exp Zool A Comp Exp Biol 2006; 305:538-550. [PMID: 16703619]
11. Henry JJ, Elkins MB. Cornea-lens transdifferentiation in the anuran, Xenopus tropicalis. Dev Genes Evol 2001; 211:377-387. [PMID: 11685571]
12. Gwon AE, Gruber LJ, Mundwiler KE. A histologic study of lens regeneration in aphakic rabbits. Invest Ophthalmol Vis Sci 1990; 31:540-547. [PMID: 2318593]
13. Lois N, Dawson R, McKinnon AD, Forrester JV. A new model of posterior capsule opacification in rodents. Invest Ophthalmol Vis Sci 2003; 44:3450-3457. [PMID: 12882794]
14. Call MK, Grogg MW, Del Rio-Tsonis K, Tsonis PA. Lens regeneration in mice: implications in cataracts. Exp Eye Res 2004; 78:297-299. [PMID: 14729361]
15. Piatigorsky J. Lens crystallins. Innovation associated with changes in gene regulation. J Biol Chem 1992; 267:4277-4280. [PMID: 1537817]
16. Altmann CR, Chow RL, Lang RA, Hemmati-Brivanlou A. Lens induction by Pax-6 in Xenopus laevis. Dev Biol 1997; 185:119-123. [PMID: 9169055]
17. McDevitt DS, Brahma SK. Ontogeny and localization of the crystallins during embryonic lens development in Xenopus laevis. J Exp Zool 1973; 186:127-140. [PMID: 4201078]
18. Brunekreef GA, van Genesen ST, Destree OH, Lubsen NH. Extralenticular expression of Xenopus laevis alpha-, beta-, and gamma-crystallin genes. Invest Ophthalmol Vis Sci 1997; 38:2764-2771. [PMID: 9418729]
19. Brahma SK, McDevitt DS. Ontogeny and localization of the lens crystallins in Xenopus laevis lens regeneration. J Embryol Exp Morphol 1974; 32:783-794. [PMID: 4618568]
20. Campbell JC. An Immuno-Fluorescent Study of Lens Regeneration in Larval Xenopus Laevis. J Embryol Exp Morphol 1965; 13:171-179. [PMID: 14329486]
21. McDevitt DS, Brahma SK. Ontogeny and localization of the alpha, beta, and gamma crystallins in newt eye lens development. Dev Biol 1981; 84:449-454. [PMID: 20737883]
22. Mizuno N, Mochii M, Takahashi TC, Eguchi G, Okada TS. Lens regeneration in Xenopus is not a mere repeat of lens development, with respect to crystallin gene expression. Differentiation 1999; 64:143-149. [PMID: 10234811]
23. Henry JJ. The cellular and molecular bases of vertebrate lens regeneration. Int Rev Cytol 2003; 228:195-265. [PMID: 14667045]
24. Filbin MT. How inflammation promotes regeneration. Nat Neurosci 2006; 9:715-717. [PMID: 16732197]
25. Leon S, Yin Y, Nguyen J, Irwin N, Benowitz LI. Lens injury stimulates axon regeneration in the mature rat optic nerve. J Neurosci 2000; 20:4615-4626. [PMID: 10844031]
26. Brockes JP, Kumar A, Velloso CP. Regeneration as an evolutionary variable. J Anat 2001; 199:3-11. [PMID: 11523827]
27. Harty M, Neff AW, King MW, Mescher AL. Regeneration or scarring: an immunologic perspective. Dev Dyn 2003; 226:268-279. [PMID: 12557205]
28. Godwin JW, Brockes JP. Regeneration, tissue injury and the immune response. J Anat 2006; 209:423-432. [PMID: 17005015]
29. Brockes JP, Kumar A. Comparative aspects of animal regeneration. Annu Rev Cell Dev Biol 2008; 24:525-549. [PMID: 18598212]
30. Yoshii C, Ueda Y, Okamoto M, Araki M. Neural retinal regeneration in the anuran amphibian Xenopus laevis postmetamorphosis: transdifferentiation of retinal pigmented epithelium regenerates the neural retina. Dev Biol 2007; 303:45-56. [PMID: 17184765]
31. Martinez-Morales JR, Signore M, Acampora D, Simeone A, Bovolenta P. Otx genes are required for tissue specification in the developing eye. Development 2001; 128:2019-2030. [PMID: 11493524]
32. Köster RW, Kuhnlein RP, Wittbrodt J. Ectopic Sox3 activity elicits sensory placode formation. Mech Dev 2000; 95:175-187. [PMID: 10906460]
33. Chow RL, Lang RA. Early eye development in vertebrates. Annu Rev Cell Dev Biol 2001; 17:255-296. [PMID: 11687490]
34. Ishibashi S, Yasuda K. Distinct roles of maf genes during Xenopus lens development. Mech Dev 2001; 101:155-166. [PMID: 11231068]
35. Ring BZ, Cordes SP, Overbeek PA, Barsh GS. Regulation of mouse lens fiber cell development and differentiation by the Maf gene. Development 2000; 127:307-317. [PMID: 10603348]
36. Cui W, Tomarev SI, Piatigorsky J, Chepelinsky AB, Duncan MK. Mafs, Prox1, and Pax6 can regulate chicken betaB1-crystallin gene expression. J Biol Chem 2004; 279:11088-11095. [PMID: 14707122]
37. Madhavan M, Haynes TL, Frisch NC, Call MK, Minich CM, Tsonis PA, Del Rio-Tsonis K. The role of Pax-6 in lens regeneration. Proc Natl Acad Sci USA 2006; 103:14848-14853. [PMID: 17003134]
38. Malloch EL, Perry KJ, Fukui L, Johnson VR, Wever J, Beck CW, King MW, Henry JJ. Gene expression profiles of lens regeneration and development in Xenopus laevis. Dev Dyn 2009; 238:2340-2356. [PMID: 19681139]
39. Henry JJ, Carinato ME, Schaefer JJ, Wolfe AD, Walter BE, Perry KJ, Elbl TN. Characterizing gene expression during lens formation in Xenopus laevis: evaluating the model for embryonic lens induction. Dev Dyn 2002; 224:168-185. [PMID: 12112470]
40. Mizuno N, Mochii M, Yamamoto TS, Takahashi TC, Eguchi G, Okada TS. Pax-6 and Prox 1 expression during lens regeneration from Cynops iris and Xenopus cornea: evidence for a genetic program common to embryonic lens development. Differentiation 1999; 65:141-149. [PMID: 10631811]
41. Mizuno N, Ueda Y, Kondoh H. Requirement for betaB1-crystallin promoter of Xenopus laevis in embryonic lens development and lens regeneration. Dev Growth Differ 2005; 47:131-140. [PMID: 15839998]
42. Walter BE, Tian Y, Garlisch AK, Carinato ME, Elkins MB, Wolfe AD, Schaefer JJ, Perry KJ, Henry JJ. Molecular profiling: gene expression reveals discrete phases of lens induction and development in Xenopus laevis. Mol Vis 2004; 10:186-198. [PMID: 15064684]
43. Nieuwkoop PD; Faber J Normal table of Xenopus laevis (daudin). New York & London: Garland Publishing, Inc 1994 [PubMed: 15064684]
44. Schaefer JJ, Oliver G, Henry JJ. Conservation of gene expression during embryonic lens formation and cornea-lens transdifferentiation in Xenopus laevis. Dev Dyn 1999; 215:308-318. [PMID: 10417820]
45. Mizuno N, Agata K, Sawada K, Mochii M, Eguchi G. Expression of crystallin genes in embryonic and regenerating newt lenses. Dev Growth Differ 2002; 44:251-256. [PMID: 12060074]
46. Ingolia TD, Craig EA. Four small Drosophila heat shock proteins are related to each other and to mammalian alphacrystallin. Proc Natl Acad Sci USA 1982; 79:2360-2364. [PMID: 6285380]
47. Jakob U, Gaestel M, Engel K, Buchner J. Small heat shock proteins are molecular chaperones. J Biol Chem 1993; 268:1517-1520. [PMID: 8093612]
48. Horwitz J. Alpha-crystallin can function as a molecular chaperone. Proc Natl Acad Sci USA 1992; 89:10449-10453. [PMID: 1438232]
49. Chen WV, Fielding Hejtmancik J, Piatigorsky J, Duncan MK. The mouse beta B1-crystallin promoter: strict regulation of lens fiber cell specificity. Biochim Biophys Acta 2001; 1519:30-38. [PMID: 11406268]
50. Shekhawat DS, Jangir OP, Prakash A, Pawan S. Lens regeneration in mice under the influence of vitamin A. J Biosci 2001; 26:571-576. [PMID: 11807287]
51. Carinato ME, Walter BE, Henry JJ. Xenopus laevis gelatinase B (Xmmp-9): development, regeneration, and wound healing. Dev Dyn 2000; 217:377-387. [PMID: 10767082]