HUSCAP logo Hokkaido Univ. logo

Hokkaido University Collection of Scholarly and Academic Papers >
Graduate School of Science / Faculty of Science >
Peer-reviewed Journal Articles, etc >

A cis-acting element in the coding region of cyclin B1 mRNA couples subcellular localization to translational timing

Files in This Item:
Yasuda_Manuscript_all.pdf9.72 MBPDFView/Open
Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/53625

Title: A cis-acting element in the coding region of cyclin B1 mRNA couples subcellular localization to translational timing
Authors: Yasuda, Kyota Browse this author
Kotani, Tomoya Browse this author →KAKEN DB
Yamashita, Masakane Browse this author →KAKEN DB
Keywords: RNA localization
Cyclin B1
Oocyte maturation
Translational control
Issue Date: 15-Oct-2013
Publisher: Academic press inc elsevier science
Journal Title: Developmental biology
Volume: 382
Issue: 2
Start Page: 517
End Page: 529
Publisher DOI: 10.1016/j.ydbio.2013.05.014
PMID: 23701882
Abstract: Subcellular localization of messenger RNAs (mRNAs) to correct sites and translational activation at appropriate timings are crucial for normal progression of various biological events. However, a molecular link between the spatial regulation and temporal regulation remains unresolved. In immature zebrafish oocytes, translationally repressed cyclin B1 mRNA is localized to the animal polar cytoplasm and its temporally regulated translational activation in response to a maturationAnducing hormone is essential to promote oocyte maturation. We previously reported that the coding region of cyclin B1 mRNA is required for the spatio-temporal regulation. Here, we report that a sequence, CAGGAGACC, that is conserved in the coding region of vertebrate cyclin B1 mRNA is involved in the regulation. Like endogenous cyclin B1 mRNA, reporter mRNAs harboring the sequence CAGGAGACC were localized to the animal polar cytoplasm of oocytes, while those carrying mutations in the sequence (with no change in the coding amino acids) were dispersed in the animal hemisphere of oocytes. Furthermore, translational activation of the mutant mRNAs was initiated at a timing earlier than that of endogenous and wild-type reporter mRNAs during oocyte maturation. Interaction of CAGGAGACC with proteins in vitro suggests that this sequence functions in collaboration with a trans-acting protein factor(s) in oocytes. These findings reveal that the sequence in the coding region of cyclin B1 mRNA plays an important role as a cis-acting element in both subcellular localization and translational timing of mRNA, providing a direct molecular link between the spatial and temporal regulation of mRNA translation. (C) 2013 Elsevier Inc. All rights reserved.
Relation: http://www.elsevier.com/wps/find/authorsview.authors/rights
http://www.sciencedirect.com/science/article/pii/S0012160613002595
Type: article (author version)
URI: http://hdl.handle.net/2115/53625
Appears in Collections:理学院・理学研究院 (Graduate School of Science / Faculty of Science) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 山下 正兼

Export metadata:

OAI-PMH ( junii2 , jpcoar_1.0 )

MathJax is now OFF:


 

 - Hokkaido University