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  Small proteins modulate ion-channel-like ACD6 to regulate immunity in Arabidopsis thaliana

Chen, J., Li, L., Kim, J., Neuhäuser, B., Wang, M., Thelen, M., et al. (2023). Small proteins modulate ion-channel-like ACD6 to regulate immunity in Arabidopsis thaliana. Molecular Cell, 83(23), 4386-4397. doi:10.1016/j.molcel.2023.10.030.

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Chen, J, Author
Li, L1, Author           
Kim, JH, Author
Neuhäuser, B, Author
Wang, M, Author
Thelen, M1, Author                 
Hilleary, R, Author
Chi, Y, Author
Wei, L, Author
Venkataramani, K1, Author                 
Exposito-Alonso, M1, Author                 
Liu, C, Author
Keck, J1, Author           
Barragan, AC1, Author                 
Schwab, R1, Author                 
Lutz, U1, Author                 
Pei, Z-M, Author
He, S-Y, Author
Ludewig, U, Author
Weigel, D1, Author                 
Zhu, W1, Author                  more..
Affiliations:
1Department Molecular Biology, Max Planck Institute for Biology Tübingen, Max Planck Society, ou_3371687              

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 Abstract: The multi-pass transmembrane protein ACCELERATED CELL DEATH 6 (ACD6) is an immune regulator in Arabidopsis thaliana with an unclear biochemical mode of action. We have identified two loci, MODULATOR OF HYPERACTIVE ACD6 1 (MHA1) and its paralog MHA1-LIKE (MHA1L), that code for ∼7 kDa proteins, which differentially interact with specific ACD6 variants. MHA1L enhances the accumulation of an ACD6 complex, thereby increasing the activity of the ACD6 standard allele for regulating plant growth and defenses. The intracellular ankyrin repeats of ACD6 are structurally similar to those found in mammalian ion channels. Several lines of evidence link increased ACD6 activity to enhanced calcium influx, with MHA1L as a direct regulator of ACD6, indicating that peptide-regulated ion channels are not restricted to animals.

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 Dates: 2023-112023-12
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1016/j.molcel.2023.10.030
PMID: 37995686
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Title: Molecular Cell
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 83 (23) Sequence Number: - Start / End Page: 4386 - 4397 Identifier: ISSN: 1097-2765
CoNE: https://pure.mpg.de/cone/journals/resource/954925610929