novel gene, fad49, plays a crucial role in the immediate early stage of adipocyte differentiation via involvement in mitotic clonal expansion
Adipogenesis is accomplished via a complex series of steps, and the events at the earliest stage remain to be elucidated. To clarify the molecular mechanisms of adipocyte differentiation, we previously isolated 102 genes expressed early in mouse 3T3-L1 preadipocyte cells using a PCR subtraction syst...
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Veröffentlicht in: | European journal of biochemistry 2008-11, Vol.275 (22), p.5576-5588 |
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creator | Hishida, Tomoaki Eguchi, Tsuyoshi Osada, Shigehiro Nishizuka, Makoto Imagawa, Masayoshi |
description | Adipogenesis is accomplished via a complex series of steps, and the events at the earliest stage remain to be elucidated. To clarify the molecular mechanisms of adipocyte differentiation, we previously isolated 102 genes expressed early in mouse 3T3-L1 preadipocyte cells using a PCR subtraction system. About half of the genes isolated appeared to be unknown. After isolating full-length cDNAs of the unknown genes, one of them, named factor for adipocyte differentiation 49 (fad49), appeared to be a novel gene, as the sequence of this clone showed no identity to known genes. FAD49 contains a phox homology (PX) domain and four Src homology 3 (SH3) domains, suggesting that it may be a novel scaffold protein. We found that the PX domain of FAD49 not only has affinity for phosphoinositides, but also binds to its third SH3 domain. Expression of fad49 was transiently elevated 3 h after differentiation was induced, and diminished 24 h after induction. Induction of the fad49 gene was observed in adipocyte differentiable 3T3-L1 cells, but not in non-adipogenic NIH-3T3 cells. RNAi-mediated knockdown of fad49 significantly impaired adipocyte differentiation. Moreover, the knockdown of fad49 by RNAi inhibited mitotic clonal expansion, and reduced the expression of CCAAT/enhancer-binding protein β (C/EBPβ) and C/EBPδ at the immediate early phase. Taken together, these results show that fad49, a novel gene, plays a crucial role in the immediate early stage of adipogenesis. |
doi_str_mv | 10.1111/j.1742-4658.2008.06682.x |
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To clarify the molecular mechanisms of adipocyte differentiation, we previously isolated 102 genes expressed early in mouse 3T3-L1 preadipocyte cells using a PCR subtraction system. About half of the genes isolated appeared to be unknown. After isolating full-length cDNAs of the unknown genes, one of them, named factor for adipocyte differentiation 49 (fad49), appeared to be a novel gene, as the sequence of this clone showed no identity to known genes. FAD49 contains a phox homology (PX) domain and four Src homology 3 (SH3) domains, suggesting that it may be a novel scaffold protein. We found that the PX domain of FAD49 not only has affinity for phosphoinositides, but also binds to its third SH3 domain. Expression of fad49 was transiently elevated 3 h after differentiation was induced, and diminished 24 h after induction. Induction of the fad49 gene was observed in adipocyte differentiable 3T3-L1 cells, but not in non-adipogenic NIH-3T3 cells. RNAi-mediated knockdown of fad49 significantly impaired adipocyte differentiation. Moreover, the knockdown of fad49 by RNAi inhibited mitotic clonal expansion, and reduced the expression of CCAAT/enhancer-binding protein β (C/EBPβ) and C/EBPδ at the immediate early phase. 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To clarify the molecular mechanisms of adipocyte differentiation, we previously isolated 102 genes expressed early in mouse 3T3-L1 preadipocyte cells using a PCR subtraction system. About half of the genes isolated appeared to be unknown. After isolating full-length cDNAs of the unknown genes, one of them, named factor for adipocyte differentiation 49 (fad49), appeared to be a novel gene, as the sequence of this clone showed no identity to known genes. FAD49 contains a phox homology (PX) domain and four Src homology 3 (SH3) domains, suggesting that it may be a novel scaffold protein. We found that the PX domain of FAD49 not only has affinity for phosphoinositides, but also binds to its third SH3 domain. Expression of fad49 was transiently elevated 3 h after differentiation was induced, and diminished 24 h after induction. Induction of the fad49 gene was observed in adipocyte differentiable 3T3-L1 cells, but not in non-adipogenic NIH-3T3 cells. RNAi-mediated knockdown of fad49 significantly impaired adipocyte differentiation. Moreover, the knockdown of fad49 by RNAi inhibited mitotic clonal expansion, and reduced the expression of CCAAT/enhancer-binding protein β (C/EBPβ) and C/EBPδ at the immediate early phase. Taken together, these results show that fad49, a novel gene, plays a crucial role in the immediate early stage of adipogenesis.</description><subject>3T3-L1 cell</subject><subject>3T3-L1 Cells</subject><subject>adipocyte differentiation</subject><subject>Adipocytes - cytology</subject><subject>Adipogenesis - genetics</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>CCAAT-Enhancer-Binding Proteins - antagonists & inhibitors</subject><subject>CCAAT/enhancer-binding protein</subject><subject>Cell Differentiation - genetics</subject><subject>Cell division</subject><subject>Cell Proliferation</subject><subject>Clone Cells - cytology</subject><subject>DNA, Complementary</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Mice</subject><subject>Mitosis</subject><subject>Molecular biology</subject><subject>Molecular Sequence Data</subject><subject>obesity</subject><subject>peroxisome proliferator-activated receptor γ</subject><subject>Phospholipid Transfer Proteins - genetics</subject><subject>Phospholipid Transfer Proteins - physiology</subject><subject>Rodents</subject><issn>1742-464X</issn><issn>0014-2956</issn><issn>1742-4658</issn><issn>1432-1033</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctu1DAUhiMEohd4BbBYsOoMjuNLvEEqVQtIlViUSuysM8nx4JETD3YyTB6Cd67DjIrEBrywj3y-81vWVxSkpMsyr3ebZak4W3Ap6iWjtF5SKWu23D8pTh8bTx9r_u2kOEtpQ2kluNbPi5Oy1kIrLk6LX33YoSdr7PGCWGi5viBbD1MiQJo4Ng48icEjcT0Zvuej67B1MCBBiH4iaYA1kmAJtG4bmik3WmctRuyHjLnQk52DPL0Lfoddvp2TOjeEwTWk8aHPD-B-C33K7IvimQWf8OXxPC_ub66_Xn1a3H75-Pnq8nbRCCnZQqxQAdVKcM64Uoi2pRVtdGW5riWUTDOwFUdgyq4qkHylJYBoBFjJtLTVefH2kLuN4ceIaTCdSw16Dz2GMRmpFavz9k-wzGBZcZnBN3-BmzDG_LlkGOVUC8VEhuoD1MSQUkRrttF1ECdTUjOLNRszOzOzPzOLNb_Fmn0efXXMH1fZwJ_Bo8kMvD8AP53H6b-Dzc31h7u5zAGvDwEWgoF1dMnc3zFaVrQUSjEqqwfslbxd</recordid><startdate>200811</startdate><enddate>200811</enddate><creator>Hishida, Tomoaki</creator><creator>Eguchi, Tsuyoshi</creator><creator>Osada, Shigehiro</creator><creator>Nishizuka, Makoto</creator><creator>Imagawa, Masayoshi</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><scope>FBQ</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200811</creationdate><title>novel gene, fad49, plays a crucial role in the immediate early stage of adipocyte differentiation via involvement in mitotic clonal expansion</title><author>Hishida, Tomoaki ; Eguchi, Tsuyoshi ; Osada, Shigehiro ; Nishizuka, Makoto ; Imagawa, Masayoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5662-5be7a0975442477eefd030c93f4986a1292af34ea27fb3a64b96aa5c5af6296f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>3T3-L1 cell</topic><topic>3T3-L1 Cells</topic><topic>adipocyte differentiation</topic><topic>Adipocytes - cytology</topic><topic>Adipogenesis - genetics</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>CCAAT-Enhancer-Binding Proteins - antagonists & inhibitors</topic><topic>CCAAT/enhancer-binding protein</topic><topic>Cell Differentiation - genetics</topic><topic>Cell division</topic><topic>Cell Proliferation</topic><topic>Clone Cells - cytology</topic><topic>DNA, Complementary</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Mice</topic><topic>Mitosis</topic><topic>Molecular biology</topic><topic>Molecular Sequence Data</topic><topic>obesity</topic><topic>peroxisome proliferator-activated receptor γ</topic><topic>Phospholipid Transfer Proteins - genetics</topic><topic>Phospholipid Transfer Proteins - physiology</topic><topic>Rodents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hishida, Tomoaki</creatorcontrib><creatorcontrib>Eguchi, Tsuyoshi</creatorcontrib><creatorcontrib>Osada, Shigehiro</creatorcontrib><creatorcontrib>Nishizuka, Makoto</creatorcontrib><creatorcontrib>Imagawa, Masayoshi</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hishida, Tomoaki</au><au>Eguchi, Tsuyoshi</au><au>Osada, Shigehiro</au><au>Nishizuka, Makoto</au><au>Imagawa, Masayoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>novel gene, fad49, plays a crucial role in the immediate early stage of adipocyte differentiation via involvement in mitotic clonal expansion</atitle><jtitle>European journal of biochemistry</jtitle><addtitle>FEBS J</addtitle><date>2008-11</date><risdate>2008</risdate><volume>275</volume><issue>22</issue><spage>5576</spage><epage>5588</epage><pages>5576-5588</pages><issn>1742-464X</issn><issn>0014-2956</issn><eissn>1742-4658</eissn><eissn>1432-1033</eissn><abstract>Adipogenesis is accomplished via a complex series of steps, and the events at the earliest stage remain to be elucidated. To clarify the molecular mechanisms of adipocyte differentiation, we previously isolated 102 genes expressed early in mouse 3T3-L1 preadipocyte cells using a PCR subtraction system. About half of the genes isolated appeared to be unknown. After isolating full-length cDNAs of the unknown genes, one of them, named factor for adipocyte differentiation 49 (fad49), appeared to be a novel gene, as the sequence of this clone showed no identity to known genes. FAD49 contains a phox homology (PX) domain and four Src homology 3 (SH3) domains, suggesting that it may be a novel scaffold protein. We found that the PX domain of FAD49 not only has affinity for phosphoinositides, but also binds to its third SH3 domain. Expression of fad49 was transiently elevated 3 h after differentiation was induced, and diminished 24 h after induction. Induction of the fad49 gene was observed in adipocyte differentiable 3T3-L1 cells, but not in non-adipogenic NIH-3T3 cells. RNAi-mediated knockdown of fad49 significantly impaired adipocyte differentiation. Moreover, the knockdown of fad49 by RNAi inhibited mitotic clonal expansion, and reduced the expression of CCAAT/enhancer-binding protein β (C/EBPβ) and C/EBPδ at the immediate early phase. Taken together, these results show that fad49, a novel gene, plays a crucial role in the immediate early stage of adipogenesis.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>18959745</pmid><doi>10.1111/j.1742-4658.2008.06682.x</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3T3-L1 cell 3T3-L1 Cells adipocyte differentiation Adipocytes - cytology Adipogenesis - genetics Animals Biochemistry CCAAT-Enhancer-Binding Proteins - antagonists & inhibitors CCAAT/enhancer-binding protein Cell Differentiation - genetics Cell division Cell Proliferation Clone Cells - cytology DNA, Complementary Gene expression Gene Expression Regulation Mice Mitosis Molecular biology Molecular Sequence Data obesity peroxisome proliferator-activated receptor γ Phospholipid Transfer Proteins - genetics Phospholipid Transfer Proteins - physiology Rodents |
title | novel gene, fad49, plays a crucial role in the immediate early stage of adipocyte differentiation via involvement in mitotic clonal expansion |
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