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Cited by 206

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Differential Arginylation of Actin Isoforms Is Regulated by Coding Sequence–Dependent Degradation

Open access
Zhang, Fangliang, Saha, Sougata, Shabalina, Svetlana A., Kashina, Anna·2010·Science

Abstract

Making Modifications: Arginylation of β-actin regulates cell motility and the actin cytoskeleton, but how differential arginylation of the two highly similar actin isoforms—β and γ—is achieved in vivo is unclear. Zhang et al. (p. 1534 ; see the Perspective by Weygand-Durasevic and Ibba ) describe a cotranslational mechanism that selectively regulates the arginylation of proteins through degradation and is dependent on the nucleotide coding sequence coupled to the translation speed. The work provides an explanation for the different N-terminal arginylation states of β- and γ-actin in vivo and suggests translation rate affected by nucleotide coding sequence confers different posttranslational states to proteins and selectively regulates protein degradation.

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Crossref · 10.1126/science.1191701

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Metadata

Authors
Zhang, F., Saha, S., Shabalina, S. A., & Kashina, A.
Venue
Science
Published
2010-09-17
Volume
329
Issue
5998
Pages
1534-1537
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2035557248
Cited by
206
References
1
FWCI
6.62
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Differential Arginylation of Actin Isoforms Is Regulated by Coding Sequence–Dependent Degradation. https://app.cochat.ai/papers/10.1126/science.1191701
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Zhang, F., Saha, S., Shabalina, S. A., & Kashina, A. (2010). Differential Arginylation of Actin Isoforms Is Regulated by Coding Sequence–Dependent Degradation. Science. https://doi.org/10.1126/science.1191701

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.