Cardiolipin and phosphatidylinositol along with the latter's phosphorylated derivative phosphoinositides, control a wide range of cellular functions from signal transduction, membrane traffic, mitochondrial function, cytoskeletal dynamics, and cell metabolism. An emerging dimension to these lipids is the specificity of their fatty acyl chains that is remarkably distinct from that of other glycerophospholipids. Cardiolipin and phosphatidylinositol undergo acyl remodeling involving the sequential actions of phospholipase A to hydrolyze acyl chains and key acyltransferases that re-acylate with specific acyl groups. LCLAT1 (also known as LYCAT, AGPAT8, LPLAT6, or ALCAT1) is an acyltransferase that contributes to specific acyl profiles for phosphatidylinositol, phosphoinositides, and cardiolipin. As such, perturbations of LCLAT1 lead to alterations in cardiolipin-dependent phenomena such as mitochondrial respiration and dynamics and phosphoinositide-dependent processes such as endocytic membrane traffic and receptor signaling. Here we examine the biochemical and cellular actions of LCLAT1, as well as the contribution of this acyltransferase to the development and specific diseases.
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October 2023
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In this issue by Vogt and colleagues (pp. 1789–1800) review how recently determined structures shed light on how NHEJ complexes function at DNA DSBs, emphasizing how multiple structures containing the DNA-dependent protein kinase catalytic subunit (DNA-PKcs) may function in NHEJ. The cover image shows the overall structure of DNA-PKcs. Image courtesy of Susan Lees-Miller.
Review Article|
September 22 2023
A tail of their own: regulation of cardiolipin and phosphatidylinositol fatty acyl profile by the acyltransferase LCLAT1
Kai Zhang;
Kai Zhang
*
1Department of Chemistry and Biology, Toronto Metropolitan University, Toronto, Ontario, Canada M5B 2K3
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Victoria Chan;
Victoria Chan
*
1Department of Chemistry and Biology, Toronto Metropolitan University, Toronto, Ontario, Canada M5B 2K3
2Graduate Program in Molecular Science, Toronto Metropolitan University, Toronto, Ontario, Canada M5B 2K3
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Roberto J. Botelho;
1Department of Chemistry and Biology, Toronto Metropolitan University, Toronto, Ontario, Canada M5B 2K3
2Graduate Program in Molecular Science, Toronto Metropolitan University, Toronto, Ontario, Canada M5B 2K3
Correspondence: Roberto J. Botelho (rbotelho@torontomu.ca) or Costin N. Antonescu (cantonescu@torontomu.ca)
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Costin N. Antonescu
1Department of Chemistry and Biology, Toronto Metropolitan University, Toronto, Ontario, Canada M5B 2K3
2Graduate Program in Molecular Science, Toronto Metropolitan University, Toronto, Ontario, Canada M5B 2K3
Correspondence: Roberto J. Botelho (rbotelho@torontomu.ca) or Costin N. Antonescu (cantonescu@torontomu.ca)
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Publisher: Portland Press Ltd
Received:
May 30 2023
Revision Received:
August 17 2023
Accepted:
September 07 2023
Online ISSN: 1470-8752
Print ISSN: 0300-5127
© 2023 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society
2023
Biochem Soc Trans (2023) 51 (5): 1765–1776.
Article history
Received:
May 30 2023
Revision Received:
August 17 2023
Accepted:
September 07 2023
Citation
Kai Zhang, Victoria Chan, Roberto J. Botelho, Costin N. Antonescu; A tail of their own: regulation of cardiolipin and phosphatidylinositol fatty acyl profile by the acyltransferase LCLAT1. Biochem Soc Trans 31 October 2023; 51 (5): 1765–1776. doi: https://doi.org/10.1042/BST20220603
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