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  1. 112 医学系研究科・医学部
  2. 02 分子細胞生物学専攻
  3. 1120220 博士論文(分子細胞生物学専攻)
  1. 0 資料タイプ別
  2. 20 学位論文
  3. 021 博士論文

Discovery of a novel lysophospholipid acyltransferase family essential for membrane asymmetry and diversity

https://doi.org/10.15083/00002323
e08e80ec-c560-4be8-9897-1e3faafbaf32
名前 / ファイル ライセンス アクション
41_hishikawa.pdf 41_hishikawa.pdf (8.2 MB)
Item type 学位論文 / Thesis or Dissertation(1)
公開日 2012-03-01
タイトル
タイトル Discovery of a novel lysophospholipid acyltransferase family essential for membrane asymmetry and diversity
言語
言語 eng
資源タイプ
資源 http://purl.org/coar/resource_type/c_46ec
タイプ thesis
ID登録
ID登録 10.15083/00002323
ID登録タイプ JaLC
その他のタイトル
その他のタイトル 生体膜の非対称性および多様性に重要な新規リゾリン脂質アシル基転移酵素ファミリーの発見
著者 菱川, 大介

× 菱川, 大介

WEKO 6531

菱川, 大介

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著者所属
著者所属 東京大学大学院医学系研究科分子細胞生物学専攻
Abstract
内容記述タイプ Abstract
内容記述 In addition to important structural and functional components of the cellular membrane, membrane phospholipids are important as a source of various lipid mediators. The fatty acid species in the membrane phospholipids are diverse depending on the polar head group of phospholipids and tissues. In glycerophospholipids, polyunsaturated fatty acids (PUFA) such as arachidonic acid or eicosapentaenoic acid, are located in an asymmetrical manner, being found at the sn-2 position of the glycerol backbone, but not at the sn-1 position. The asymmetrical properties of membrane phospholipids are important for membrane flexibility, fluidity and curvature. The rapid turnover of the sn-2 acyl moiety of glycerophospholipids was described in 1958 as a remodeling pathway, known as the Lands’ cycle, and is due to the concerted activities of phospholipase A2s (PLA2s) and lysophospholipid acyltransferases (LPLATs). The exclusive presence of an unsaturated fatty acid at the sn-2 position of membrane phospholipids is maintained in the remodeling pathway. However, the molecular mechanisms and biological significance of this remodeling pathway have remained for a long time elusive. Here, I report the discovery of a new acyltransferase family called the membrane bound O-acyltransferase (MBOAT) family. Within this family, I identified three enzymes that catalyze the transfer of various types of acyl-CoAs to lysophospholipids to produce different classes of phospholipids. These enzymes showed different tissue distributions and substrate specificities; one termed lysophosphatidylcholine acyltransferase-3 (LPCAT3) prefers arachidonoyl-CoA, and the other 2 enzymes, which termed LPCAT4 and LPEAT1, incorporate oleoyl-CoAs into lysophospholipids. Importantly, siRNA specific for LPCAT3 reduced endogenous LPLAT activities and the amount of phospholipids containing PUFA at the sn-2 position. Thus, I propose that the diversity of membrane glycerophospholipids is produced by the concerted and overlapping activities of multiple enzymes that recognize both the polar head group of glycerophospholipids and various acyl-CoAs
書誌情報 発行日 2009-03-23
学位名
学位名 博士(医学)
学位
値 doctoral
学位分野
Medical Science (医学)
学位授与機関
学位授与機関名
学位授与機関名 University of Tokyo (東京大学)
研究科・専攻
Department of Molecular Cell Biology, Graduate School of Medicine (医学系研究科分子細胞生物学専攻)
学位授与年月日
学位授与年月日 2009-03-23
学位授与番号
学位授与番号 甲第24766号
学位記番号
博医第3186号
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