Evidence map›Paper›PMID 21527991›Full record

ArticleMolecular vision2011

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

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

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Article in Molecular vision, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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3 · Its place in the literature

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4 citing papers in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Yongqing ZhaoSchool of Life Sciences, Lanzhou University, Lanzhou, Gansu, China.
Furong Ju
Yuanlin Zhao
Lei Wang
Zhenglong Sun
Mingxin Liu
Lan Gao

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo explore the expression of the lens crystallins (αA- and βB1-crystallin) in Xenopus laevis embryonic lens development and regeneration and to analyze the order of different crystallins generated in the regenerating lens.

methodsReal Time-PCR, Immunofluorescence, and 2D-PAGE were used to analyze the expressions of αA-crystallin and βB1-crystallin, and related factors during embryonic lens development and regeneration in Xenopus laevis.

resultsαA-crystallin and βB1-crystallin were first detected at stage 29/30 during normal development, and the two crystallins were simultaneously detected in regeneration. During embryonic lens development, the relative expression level of the βB1-crystallin gene was higher than that of the αA-crystallin gene. In the process of the lens regeneration, however, the relative expression level of the βB1-crystallin gene was lower than that of the αA-crystallin gene. Throughout embryonic lens development, the two crystallin transcripts showed the same variation trends, and similar occurrence did in the regeneration process. Crystallins showed different localization and distribution during the ontogeny and regeneration, especially in the lens fiber region. 2D-electrophores revealed the patterns of the sequential synthesis of crystallins, with regard to the different classes and apparent variations of some auxiliary regulatory factors.

conclusionsThe ontogeny and localization of the crystallins during embryonic lens development and regeneration indicated a different development program, although they have identical origins, the ectoderm. The expression level of crystallin transcripts displayed a consistent variation tendency, but the presence of appreciable differences was still exposed. In addition to stably producing the crystallins of different classes in accordance with established procedure, these auxiliary factors may perform the function, to some extent, because of significant changes in their expression throughout the process of lens regeneration.

Indexed as

Gene Expression Regulation, Developmentalalpha-Crystallin A ChainAnimalsbeta-Crystallin B ChainCloning, MolecularEctodermElectrophoresis, Gel, Two-DimensionalEmbryonic DevelopmentEmbryo, NonmammalianEscherichia coliIn Situ HybridizationLens, CrystallinePolymerase Chain ReactionProteomicsRecombinant ProteinsRegenerationalpha-Crystallin A Chainbeta-Crystallin B ChainRecombinant ProteinsRNA, Messenger

Identifiers

PMID21527991
PMCPMC3081792

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.