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An alternative spliced mouse presenilin-2 mRNA encodes a novel γ-secretase inhibitor

The γ-secretase, composed of presenilin-1 (PS1) or presenilin-2 (PS2), nicastrin (NCT), anterior pharynx-defective phenotype 1 (APH-1), and PEN-2, is critical for the development of Alzheimer’s disease (AD). PSs are autoproteolytically cleaved, producing an N-terminal fragment (NTF) and a hydrophili...

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Published in:FEBS letters 2009-05, Vol.583 (9), p.1403-1408
Main Authors: Suzuki, Yoshihiro, Ohta, Kazunori, Itoh, Masanori, Sakoh-Sumitomo, Yukari, Mitsuda, Teruhiko, Ueda, Masashi, Hayakawa-Yano, Yoshika, Li, Shimo, Hida, Yoko, Inuzuka, Takashi, Jung, Yong-Keun, Nakagawa, Toshiyuki
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cited_by cdi_FETCH-LOGICAL-c5060-a33de98536acc2755a3997b82a5f0ceff219fec47e2bb16cfc45de9c8b185dcc3
cites cdi_FETCH-LOGICAL-c5060-a33de98536acc2755a3997b82a5f0ceff219fec47e2bb16cfc45de9c8b185dcc3
container_end_page 1408
container_issue 9
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container_title FEBS letters
container_volume 583
creator Suzuki, Yoshihiro
Ohta, Kazunori
Itoh, Masanori
Sakoh-Sumitomo, Yukari
Mitsuda, Teruhiko
Ueda, Masashi
Hayakawa-Yano, Yoshika
Li, Shimo
Hida, Yoko
Inuzuka, Takashi
Jung, Yong-Keun
Nakagawa, Toshiyuki
description The γ-secretase, composed of presenilin-1 (PS1) or presenilin-2 (PS2), nicastrin (NCT), anterior pharynx-defective phenotype 1 (APH-1), and PEN-2, is critical for the development of Alzheimer’s disease (AD). PSs are autoproteolytically cleaved, producing an N-terminal fragment (NTF) and a hydrophilic loop domain-containing C-terminal fragment. However, the role of the loop domain in the γ-secretase complex assembly remains unknown. Here, we report a novel PS2 isoform generated by alternative splicing, named PS2β, which is composed of an NTF with a hydrophilic loop domain. PS2β disturbed the interaction between NCT and APH-1, resulting in the inhibition of amyloid-β production. We concluded that PS2β may inhibit γ-secretase activity by affecting the γ-secretase complex assembly. MINT- 7025654: APH1 (uniprotkb: Q96BI3) physically interacts (MI: 0218) with PEN2 (uniprotkb: Q9NZ42), PS2 beta (uniprotkb: Q61144-2) and PS1 (uniprotkb: P49769) by anti tag coimmunoprecipitation (MI: 0007) MINT- 7025631: APH1 (uniprotkb: Q96BI3) physically interacts (MI: 0218) with NCT (uniprotkb: Q92542), PEN2 (uniprotkb: Q9NZ42) and PS1 (uniprotkb: P49769) by anti tag coimmunoprecipitation (MI: 0007)
doi_str_mv 10.1016/j.febslet.2009.04.014
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PSs are autoproteolytically cleaved, producing an N-terminal fragment (NTF) and a hydrophilic loop domain-containing C-terminal fragment. However, the role of the loop domain in the γ-secretase complex assembly remains unknown. Here, we report a novel PS2 isoform generated by alternative splicing, named PS2β, which is composed of an NTF with a hydrophilic loop domain. PS2β disturbed the interaction between NCT and APH-1, resulting in the inhibition of amyloid-β production. We concluded that PS2β may inhibit γ-secretase activity by affecting the γ-secretase complex assembly. MINT- 7025654: APH1 (uniprotkb: Q96BI3) physically interacts (MI: 0218) with PEN2 (uniprotkb: Q9NZ42), PS2 beta (uniprotkb: Q61144-2) and PS1 (uniprotkb: P49769) by anti tag coimmunoprecipitation (MI: 0007) MINT- 7025631: APH1 (uniprotkb: Q96BI3) physically interacts (MI: 0218) with NCT (uniprotkb: Q92542), PEN2 (uniprotkb: Q9NZ42) and PS1 (uniprotkb: P49769) by anti tag coimmunoprecipitation (MI: 0007)</description><identifier>ISSN: 0014-5793</identifier><identifier>EISSN: 1873-3468</identifier><identifier>DOI: 10.1016/j.febslet.2009.04.014</identifier><identifier>PMID: 19376115</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>3-cholamidopropyl dimethylammonio propanesulfonic acid ; Alternative Splicing ; Alzheimer's disease ; Amyloid Precursor Protein Secretases - antagonists &amp; inhibitors ; Amyloid-β ; Animals ; anterior pharynx-defective phenotype 1 ; APH-1 ; Base Sequence ; CHAPS ; Cloning, Molecular ; DNA, Complementary ; Enzyme Inhibitors ; Humans ; Mice ; Molecular Sequence Data ; monomeric red fluorescence protein ; mRFP ; NCT ; Nicastrin ; PEN-2 ; Presenilin ; presenilin enhancer 2 ; Presenilin-2 - chemistry ; Presenilin-2 - genetics ; Presenilin-2 - physiology ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Homology, Nucleic Acid ; γ-Secretase</subject><ispartof>FEBS letters, 2009-05, Vol.583 (9), p.1403-1408</ispartof><rights>2009</rights><rights>FEBS Letters 583 (2009) 1873-3468 © 2015 Federation of European Biochemical Societies</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5060-a33de98536acc2755a3997b82a5f0ceff219fec47e2bb16cfc45de9c8b185dcc3</citedby><cites>FETCH-LOGICAL-c5060-a33de98536acc2755a3997b82a5f0ceff219fec47e2bb16cfc45de9c8b185dcc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014579309002890$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3547,27923,27924,45779</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19376115$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suzuki, Yoshihiro</creatorcontrib><creatorcontrib>Ohta, Kazunori</creatorcontrib><creatorcontrib>Itoh, Masanori</creatorcontrib><creatorcontrib>Sakoh-Sumitomo, Yukari</creatorcontrib><creatorcontrib>Mitsuda, Teruhiko</creatorcontrib><creatorcontrib>Ueda, Masashi</creatorcontrib><creatorcontrib>Hayakawa-Yano, Yoshika</creatorcontrib><creatorcontrib>Li, Shimo</creatorcontrib><creatorcontrib>Hida, Yoko</creatorcontrib><creatorcontrib>Inuzuka, Takashi</creatorcontrib><creatorcontrib>Jung, Yong-Keun</creatorcontrib><creatorcontrib>Nakagawa, Toshiyuki</creatorcontrib><title>An alternative spliced mouse presenilin-2 mRNA encodes a novel γ-secretase inhibitor</title><title>FEBS letters</title><addtitle>FEBS Lett</addtitle><description>The γ-secretase, composed of presenilin-1 (PS1) or presenilin-2 (PS2), nicastrin (NCT), anterior pharynx-defective phenotype 1 (APH-1), and PEN-2, is critical for the development of Alzheimer’s disease (AD). PSs are autoproteolytically cleaved, producing an N-terminal fragment (NTF) and a hydrophilic loop domain-containing C-terminal fragment. However, the role of the loop domain in the γ-secretase complex assembly remains unknown. Here, we report a novel PS2 isoform generated by alternative splicing, named PS2β, which is composed of an NTF with a hydrophilic loop domain. PS2β disturbed the interaction between NCT and APH-1, resulting in the inhibition of amyloid-β production. We concluded that PS2β may inhibit γ-secretase activity by affecting the γ-secretase complex assembly. MINT- 7025654: APH1 (uniprotkb: Q96BI3) physically interacts (MI: 0218) with PEN2 (uniprotkb: Q9NZ42), PS2 beta (uniprotkb: Q61144-2) and PS1 (uniprotkb: P49769) by anti tag coimmunoprecipitation (MI: 0007) MINT- 7025631: APH1 (uniprotkb: Q96BI3) physically interacts (MI: 0218) with NCT (uniprotkb: Q92542), PEN2 (uniprotkb: Q9NZ42) and PS1 (uniprotkb: P49769) by anti tag coimmunoprecipitation (MI: 0007)</description><subject>3-cholamidopropyl dimethylammonio propanesulfonic acid</subject><subject>Alternative Splicing</subject><subject>Alzheimer's disease</subject><subject>Amyloid Precursor Protein Secretases - antagonists &amp; inhibitors</subject><subject>Amyloid-β</subject><subject>Animals</subject><subject>anterior pharynx-defective phenotype 1</subject><subject>APH-1</subject><subject>Base Sequence</subject><subject>CHAPS</subject><subject>Cloning, Molecular</subject><subject>DNA, Complementary</subject><subject>Enzyme Inhibitors</subject><subject>Humans</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>monomeric red fluorescence protein</subject><subject>mRFP</subject><subject>NCT</subject><subject>Nicastrin</subject><subject>PEN-2</subject><subject>Presenilin</subject><subject>presenilin enhancer 2</subject><subject>Presenilin-2 - chemistry</subject><subject>Presenilin-2 - genetics</subject><subject>Presenilin-2 - physiology</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>γ-Secretase</subject><issn>0014-5793</issn><issn>1873-3468</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkc1u1DAURi0EokPhEUBesUu4_kvsFRqqliJVRWrp2nKcG-GRkwx2ZlCfq-_BM-HRjMSyrCxb5_tsn0vIewY1A9Z82tQDdjniUnMAU4OsgckXZMV0KyohG_2SrKAcVao14oy8yXkDZa-ZeU3OmBFtw5hakYf1RF1cME1uCXukeRuDx56O8y4j3SbMOIUYporT8e52TXHyc4-ZOjrNe4z0z1OV0SdcXMHD9DN0YZnTW_JqcDHju9N6Th6uLn9cXFc3379-u1jfVF5BA5UTokejlWic97xVyglj2k5zpwbwOAycmQG9bJF3HWv84KUqAa87plXvvTgnH4-92zT_2mFe7BiyxxjdhOUDtmmZ5iD1syBnTELDZQHVEfRpzjnhYLcpjC49Wgb2IN5u7Em8PYi3IG2xXHIfThfsuhH7f6mT6QJcH4HfIeLj_7Xaq8sv_P4wxcMQwQBwbaBUfT5WYVG7D5hs9qEMBvuQ0C-2n8Mzr_0LG6utxA</recordid><startdate>20090506</startdate><enddate>20090506</enddate><creator>Suzuki, Yoshihiro</creator><creator>Ohta, Kazunori</creator><creator>Itoh, Masanori</creator><creator>Sakoh-Sumitomo, Yukari</creator><creator>Mitsuda, Teruhiko</creator><creator>Ueda, Masashi</creator><creator>Hayakawa-Yano, Yoshika</creator><creator>Li, Shimo</creator><creator>Hida, Yoko</creator><creator>Inuzuka, Takashi</creator><creator>Jung, Yong-Keun</creator><creator>Nakagawa, Toshiyuki</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>20090506</creationdate><title>An alternative spliced mouse presenilin-2 mRNA encodes a novel γ-secretase inhibitor</title><author>Suzuki, Yoshihiro ; 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PSs are autoproteolytically cleaved, producing an N-terminal fragment (NTF) and a hydrophilic loop domain-containing C-terminal fragment. However, the role of the loop domain in the γ-secretase complex assembly remains unknown. Here, we report a novel PS2 isoform generated by alternative splicing, named PS2β, which is composed of an NTF with a hydrophilic loop domain. PS2β disturbed the interaction between NCT and APH-1, resulting in the inhibition of amyloid-β production. We concluded that PS2β may inhibit γ-secretase activity by affecting the γ-secretase complex assembly. MINT- 7025654: APH1 (uniprotkb: Q96BI3) physically interacts (MI: 0218) with PEN2 (uniprotkb: Q9NZ42), PS2 beta (uniprotkb: Q61144-2) and PS1 (uniprotkb: P49769) by anti tag coimmunoprecipitation (MI: 0007) MINT- 7025631: APH1 (uniprotkb: Q96BI3) physically interacts (MI: 0218) with NCT (uniprotkb: Q92542), PEN2 (uniprotkb: Q9NZ42) and PS1 (uniprotkb: P49769) by anti tag coimmunoprecipitation (MI: 0007)</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>19376115</pmid><doi>10.1016/j.febslet.2009.04.014</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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ispartof FEBS letters, 2009-05, Vol.583 (9), p.1403-1408
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source ScienceDirect Journals; Wiley-Blackwell Read & Publish Collection
subjects 3-cholamidopropyl dimethylammonio propanesulfonic acid
Alternative Splicing
Alzheimer's disease
Amyloid Precursor Protein Secretases - antagonists & inhibitors
Amyloid-β
Animals
anterior pharynx-defective phenotype 1
APH-1
Base Sequence
CHAPS
Cloning, Molecular
DNA, Complementary
Enzyme Inhibitors
Humans
Mice
Molecular Sequence Data
monomeric red fluorescence protein
mRFP
NCT
Nicastrin
PEN-2
Presenilin
presenilin enhancer 2
Presenilin-2 - chemistry
Presenilin-2 - genetics
Presenilin-2 - physiology
Reverse Transcriptase Polymerase Chain Reaction
Sequence Homology, Nucleic Acid
γ-Secretase
title An alternative spliced mouse presenilin-2 mRNA encodes a novel γ-secretase inhibitor
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