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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 |
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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 |
format | article |
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7025654:
APH1 (uniprotkb:
Q96BI3)
physically interacts (MI:
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Q9NZ42),
PS2 beta (uniprotkb:
Q61144-2) and
PS1 (uniprotkb:
P49769) by
anti tag coimmunoprecipitation (MI:
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MINT-
7025631:
APH1 (uniprotkb:
Q96BI3)
physically interacts (MI:
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NCT (uniprotkb:
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PEN2 (uniprotkb:
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anti tag coimmunoprecipitation (MI:
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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:
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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 & 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 ; 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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5060-a33de98536acc2755a3997b82a5f0ceff219fec47e2bb16cfc45de9c8b185dcc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>3-cholamidopropyl dimethylammonio propanesulfonic acid</topic><topic>Alternative Splicing</topic><topic>Alzheimer's disease</topic><topic>Amyloid Precursor Protein Secretases - antagonists & inhibitors</topic><topic>Amyloid-β</topic><topic>Animals</topic><topic>anterior pharynx-defective phenotype 1</topic><topic>APH-1</topic><topic>Base Sequence</topic><topic>CHAPS</topic><topic>Cloning, Molecular</topic><topic>DNA, Complementary</topic><topic>Enzyme Inhibitors</topic><topic>Humans</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>monomeric red fluorescence protein</topic><topic>mRFP</topic><topic>NCT</topic><topic>Nicastrin</topic><topic>PEN-2</topic><topic>Presenilin</topic><topic>presenilin enhancer 2</topic><topic>Presenilin-2 - chemistry</topic><topic>Presenilin-2 - genetics</topic><topic>Presenilin-2 - physiology</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>γ-Secretase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suzuki, Yoshihiro</au><au>Ohta, Kazunori</au><au>Itoh, Masanori</au><au>Sakoh-Sumitomo, Yukari</au><au>Mitsuda, Teruhiko</au><au>Ueda, Masashi</au><au>Hayakawa-Yano, Yoshika</au><au>Li, Shimo</au><au>Hida, Yoko</au><au>Inuzuka, Takashi</au><au>Jung, Yong-Keun</au><au>Nakagawa, Toshiyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An alternative spliced mouse presenilin-2 mRNA encodes a novel γ-secretase inhibitor</atitle><jtitle>FEBS letters</jtitle><addtitle>FEBS Lett</addtitle><date>2009-05-06</date><risdate>2009</risdate><volume>583</volume><issue>9</issue><spage>1403</spage><epage>1408</epage><pages>1403-1408</pages><issn>0014-5793</issn><eissn>1873-3468</eissn><abstract>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)</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> |
fulltext | fulltext |
identifier | ISSN: 0014-5793 |
ispartof | FEBS letters, 2009-05, Vol.583 (9), p.1403-1408 |
issn | 0014-5793 1873-3468 |
language | eng |
recordid | cdi_proquest_miscellaneous_67182048 |
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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