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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Genes to Cellsarrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Genes to Cells
Article . 2000 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
Genes to Cells
Article . 2000
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Identification and characterization of testis specific ornithine decarboxylase antizyme (OAZ‐t) gene: expression in haploid germ cells and polyamine‐induced frameshifting

Authors: Y, Tosaka; H, Tanaka; Y, Yano; K, Masai; M, Nozaki; K, Yomogida; S, Otani; +2 Authors

Identification and characterization of testis specific ornithine decarboxylase antizyme (OAZ‐t) gene: expression in haploid germ cells and polyamine‐induced frameshifting

Abstract

BackgroundPolyamines are known to play important roles in the proliferation and differentiation of many types of cells. However, in the testis, where polyamines such as spermidine and spermine exist in high concentrations, their roles still remains to be elucidated.ResultsWe have cloned a testis‐specific gene encoding an ornithine decarboxylase antizyme known to control intracellular concentrations of polyamines in a feedback manner. The mRNA encoding the protein named ornithine decarboxylase antizyme in testis (OAZ‐t) was specifically expressed in haploid germ cells. In contrast, the mRNA level of somatic ornithine decarboxylase antizyme 1 (OAZ1) decreased markedly at the late stages of haploid germ cell differentiation. OAZ‐t mRNA was first observed in 23‐day‐old mice, whereas the OAZ‐t protein was detected much later, at 35 days after birth. Further experiments on OAZ‐t revealed that polyamines were capable of inducing a frameshifting at the frameshift sequence of OAZ‐t mRNA, resulting in the translation of OAZ‐t, as was the case with the somatic OAZ1. Transfection of OAZ‐t cDNA inactivated the ornithine decarboxylase activity in the HEK293 cells.ConclusionsResults indicate that the expression of OAZ‐t is controlled at both transcriptional and translational levels, and that OAZ‐t likely plays a key role in spermatogenesis by regulating the intracellular concentration of polyamines in haploid germ cells.

Keywords

Male, DNA, Complementary, Base Sequence, Green Fluorescent Proteins, Frameshifting, Ribosomal, CHO Cells, Haploidy, Blotting, Northern, Immunohistochemistry, Cell Line, Mice, Inbred C57BL, Luminescent Proteins, Mice, Gene Expression Regulation, Cricetinae, Animals, Humans, Amino Acid Sequence, Cloning, Molecular, In Situ Hybridization

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
95
Top 10%
Top 10%
Top 10%