Similar sequences but dissimilar biological functions of GDF11 and myostatin
Growth differentiation factor 11 (GDF11) and myostatin (MSTN) are closely related TGFβ family members that are often believed to serve similar functions due to their high homology. However, genetic studies in animals provide clear evidence that they perform distinct roles. While the loss of Mstn lea...
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description | Growth differentiation factor 11 (GDF11) and myostatin (MSTN) are closely related TGFβ family members that are often believed to serve similar functions due to their high homology. However, genetic studies in animals provide clear evidence that they perform distinct roles. While the loss of
Mstn
leads to hypermuscularity, the deletion of
Gdf11
results in abnormal skeletal patterning and organ development. The perinatal lethality of
Gdf11
-null mice, which contrasts with the long-term viability of
Mstn
-null mice, has led most research to focus on utilizing recombinant GDF11 proteins to investigate the postnatal functions of GDF11. However, the reported outcomes of the exogenous application of recombinant GDF11 proteins are controversial partly because of the different sources and qualities of recombinant GDF11 used and because recombinant GDF11 and MSTN proteins are nearly indistinguishable due to their similar structural and biochemical properties. Here, we analyze the similarities and differences between GDF11 and MSTN from an evolutionary point of view and summarize the current understanding of the biological processing, signaling, and physiological functions of GDF11 and MSTN. Finally, we discuss the potential use of recombinant GDF11 as a therapeutic option for a wide range of medical conditions and the possible adverse effects of GDF11 inhibition mediated by MSTN inhibitors.
Growth factors: untangling twin proteins
A growth factor protein called GDF11 has potential for rejuvenation of heart, brain, and muscle tissues, but first its relationship with a twin growth factor (MSTN) must be unraveled. Although GDF11 and MSTN are almost identical in amino acid sequence, MSTN controls growth of skeletal muscles, and GDF11 regulates bone and organ patterning. To untangle what differentiates these proteins, Yun-Sil Lee and Joonho Suh at Seoul National University, South Korea, reviewed their evolution and function. They report that GDF11 and MSTN are the result of duplication of an original gene and have evolved to perform different roles. They cover some of the beneficial effects reported with GDF11 supplementation, such as tissue rejuvenation and increased lifespan, but caution that negative effects have been reported. Further investigation may illuminate growth and development processes, and therapeutic potential. |
doi_str_mv | 10.1038/s12276-020-00516-4 |
format | Article |
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Mstn
leads to hypermuscularity, the deletion of
Gdf11
results in abnormal skeletal patterning and organ development. The perinatal lethality of
Gdf11
-null mice, which contrasts with the long-term viability of
Mstn
-null mice, has led most research to focus on utilizing recombinant GDF11 proteins to investigate the postnatal functions of GDF11. However, the reported outcomes of the exogenous application of recombinant GDF11 proteins are controversial partly because of the different sources and qualities of recombinant GDF11 used and because recombinant GDF11 and MSTN proteins are nearly indistinguishable due to their similar structural and biochemical properties. Here, we analyze the similarities and differences between GDF11 and MSTN from an evolutionary point of view and summarize the current understanding of the biological processing, signaling, and physiological functions of GDF11 and MSTN. Finally, we discuss the potential use of recombinant GDF11 as a therapeutic option for a wide range of medical conditions and the possible adverse effects of GDF11 inhibition mediated by MSTN inhibitors.
Growth factors: untangling twin proteins
A growth factor protein called GDF11 has potential for rejuvenation of heart, brain, and muscle tissues, but first its relationship with a twin growth factor (MSTN) must be unraveled. Although GDF11 and MSTN are almost identical in amino acid sequence, MSTN controls growth of skeletal muscles, and GDF11 regulates bone and organ patterning. To untangle what differentiates these proteins, Yun-Sil Lee and Joonho Suh at Seoul National University, South Korea, reviewed their evolution and function. They report that GDF11 and MSTN are the result of duplication of an original gene and have evolved to perform different roles. They cover some of the beneficial effects reported with GDF11 supplementation, such as tissue rejuvenation and increased lifespan, but caution that negative effects have been reported. Further investigation may illuminate growth and development processes, and therapeutic potential.</description><identifier>ISSN: 1226-3613</identifier><identifier>EISSN: 2092-6413</identifier><identifier>DOI: 10.1038/s12276-020-00516-4</identifier><identifier>PMID: 33077875</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13 ; 13/100 ; 38 ; 38/1 ; 38/89 ; 631/208/182 ; 631/45/127/1219 ; 631/80/86/2368 ; 64 ; 82 ; 96 ; 96/21 ; 96/44 ; Amino acid sequence ; Biochemistry & Molecular Biology ; Biomedical and Life Sciences ; Biomedicine ; Growth differentiation factor 11 ; Growth factors ; Homology ; Information processing ; Lethality ; Life Sciences & Biomedicine ; Life span ; Medical Biochemistry ; Medicine, Research & Experimental ; Molecular Medicine ; Myostatin ; Pattern formation ; Proteins ; Research & Experimental Medicine ; Review ; Review Article ; Science & Technology ; Skeletal muscle ; Stem Cells ; Supplements ; 생화학</subject><ispartof>Experimental and Molecular Medicine, 2020, 52(0), , pp.1-21</ispartof><rights>The Author(s) 2020</rights><rights>The Author(s) 2020. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>22</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000579689200001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c574t-8b30b958e31bcf62552f1bee21f54a3f9283ca9397b8ca4764219b756ed9e2793</citedby><cites>FETCH-LOGICAL-c574t-8b30b958e31bcf62552f1bee21f54a3f9283ca9397b8ca4764219b756ed9e2793</cites><orcidid>0000-0002-1228-0404</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080601/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080601/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,729,782,786,866,887,2106,2118,27933,27934,28257,41129,42198,51585,53800,53802</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33077875$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002637475$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Suh, Joonho</creatorcontrib><creatorcontrib>Lee, Yun-Sil</creatorcontrib><title>Similar sequences but dissimilar biological functions of GDF11 and myostatin</title><title>Experimental & molecular medicine</title><addtitle>Exp Mol Med</addtitle><addtitle>EXP MOL MED</addtitle><addtitle>Exp Mol Med</addtitle><description>Growth differentiation factor 11 (GDF11) and myostatin (MSTN) are closely related TGFβ family members that are often believed to serve similar functions due to their high homology. However, genetic studies in animals provide clear evidence that they perform distinct roles. While the loss of
Mstn
leads to hypermuscularity, the deletion of
Gdf11
results in abnormal skeletal patterning and organ development. The perinatal lethality of
Gdf11
-null mice, which contrasts with the long-term viability of
Mstn
-null mice, has led most research to focus on utilizing recombinant GDF11 proteins to investigate the postnatal functions of GDF11. However, the reported outcomes of the exogenous application of recombinant GDF11 proteins are controversial partly because of the different sources and qualities of recombinant GDF11 used and because recombinant GDF11 and MSTN proteins are nearly indistinguishable due to their similar structural and biochemical properties. Here, we analyze the similarities and differences between GDF11 and MSTN from an evolutionary point of view and summarize the current understanding of the biological processing, signaling, and physiological functions of GDF11 and MSTN. Finally, we discuss the potential use of recombinant GDF11 as a therapeutic option for a wide range of medical conditions and the possible adverse effects of GDF11 inhibition mediated by MSTN inhibitors.
Growth factors: untangling twin proteins
A growth factor protein called GDF11 has potential for rejuvenation of heart, brain, and muscle tissues, but first its relationship with a twin growth factor (MSTN) must be unraveled. Although GDF11 and MSTN are almost identical in amino acid sequence, MSTN controls growth of skeletal muscles, and GDF11 regulates bone and organ patterning. To untangle what differentiates these proteins, Yun-Sil Lee and Joonho Suh at Seoul National University, South Korea, reviewed their evolution and function. They report that GDF11 and MSTN are the result of duplication of an original gene and have evolved to perform different roles. They cover some of the beneficial effects reported with GDF11 supplementation, such as tissue rejuvenation and increased lifespan, but caution that negative effects have been reported. Further investigation may illuminate growth and development processes, and therapeutic potential.</description><subject>13</subject><subject>13/100</subject><subject>38</subject><subject>38/1</subject><subject>38/89</subject><subject>631/208/182</subject><subject>631/45/127/1219</subject><subject>631/80/86/2368</subject><subject>64</subject><subject>82</subject><subject>96</subject><subject>96/21</subject><subject>96/44</subject><subject>Amino acid sequence</subject><subject>Biochemistry & Molecular Biology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Growth differentiation factor 11</subject><subject>Growth factors</subject><subject>Homology</subject><subject>Information processing</subject><subject>Lethality</subject><subject>Life Sciences & Biomedicine</subject><subject>Life span</subject><subject>Medical Biochemistry</subject><subject>Medicine, Research & Experimental</subject><subject>Molecular Medicine</subject><subject>Myostatin</subject><subject>Pattern formation</subject><subject>Proteins</subject><subject>Research & Experimental Medicine</subject><subject>Review</subject><subject>Review Article</subject><subject>Science & Technology</subject><subject>Skeletal muscle</subject><subject>Stem Cells</subject><subject>Supplements</subject><subject>생화학</subject><issn>1226-3613</issn><issn>2092-6413</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>AOWDO</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkkuP0zAUhSMEYkrhD7BAkdiAUMDvxwZpVJihUiUkGNaW7TjFncQe7AQ0_x63KYVhgVjZ8v3O8b32qaqnELyGAIs3GSLEWQMQaACgkDXkXrVAQKKGEYjvV4tSZw1mEJ9Vj3LeAYAo4eRhdYYx4Fxwuqg2n_3ge53q7L5NLliXazONdetzPhaMj33ceqv7upuCHX0MuY5dffnuAsJah7YebmMe9ejD4-pBp_vsnhzXZfXl4v3V6kOz-Xi5Xp1vGks5GRthMDCSCoehsR1DlKIOGucQ7CjRuJNIYKslltwIqwlnBEFpOGWulQ5xiZfVy9k3pE5dW6-i9od1G9V1UuefrtZKUgmwRIVdz2wb9U7dJD_odHsQHA5i2iqdRm97pwzlrBOo1aQFpOVSSstaBp2wUnBQul5Wb2evm8kMrrUujEn3d0zvVoL_Wnr6rgQQgAFYDF4cDVIsz51HNfhsXd_r4OKUFSIUUQAlEAV9_he6i1MK5VkLxSGlmEtWKDRTNsWck-tOzUCg9iFRc0hUCYk6hESRInr25xgnya9UFEDMwA9nYpet3wfjhIHiU-4WEpUdgCu___sYVnEKY5G--n9pofFM50KErUu_h_xH_z8BEIXmpg</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Suh, Joonho</creator><creator>Lee, Yun-Sil</creator><general>Nature Publishing Group UK</general><general>Springer Nature</general><general>Springer Nature B.V</general><general>Nature Publishing Group</general><general>생화학분자생물학회</general><scope>C6C</scope><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0002-1228-0404</orcidid></search><sort><creationdate>20201001</creationdate><title>Similar sequences but dissimilar biological functions of GDF11 and myostatin</title><author>Suh, Joonho ; Lee, Yun-Sil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-8b30b958e31bcf62552f1bee21f54a3f9283ca9397b8ca4764219b756ed9e2793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>13</topic><topic>13/100</topic><topic>38</topic><topic>38/1</topic><topic>38/89</topic><topic>631/208/182</topic><topic>631/45/127/1219</topic><topic>631/80/86/2368</topic><topic>64</topic><topic>82</topic><topic>96</topic><topic>96/21</topic><topic>96/44</topic><topic>Amino acid sequence</topic><topic>Biochemistry & Molecular Biology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Growth differentiation factor 11</topic><topic>Growth factors</topic><topic>Homology</topic><topic>Information processing</topic><topic>Lethality</topic><topic>Life Sciences & Biomedicine</topic><topic>Life span</topic><topic>Medical Biochemistry</topic><topic>Medicine, Research & Experimental</topic><topic>Molecular Medicine</topic><topic>Myostatin</topic><topic>Pattern formation</topic><topic>Proteins</topic><topic>Research & Experimental Medicine</topic><topic>Review</topic><topic>Review Article</topic><topic>Science & Technology</topic><topic>Skeletal muscle</topic><topic>Stem Cells</topic><topic>Supplements</topic><topic>생화학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Suh, Joonho</creatorcontrib><creatorcontrib>Lee, Yun-Sil</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><collection>Korean Citation Index</collection><jtitle>Experimental & molecular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Suh, Joonho</au><au>Lee, Yun-Sil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Similar sequences but dissimilar biological functions of GDF11 and myostatin</atitle><jtitle>Experimental & molecular medicine</jtitle><stitle>Exp Mol Med</stitle><stitle>EXP MOL MED</stitle><addtitle>Exp Mol Med</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>52</volume><issue>10</issue><spage>1673</spage><epage>1693</epage><pages>1673-1693</pages><issn>1226-3613</issn><eissn>2092-6413</eissn><abstract>Growth differentiation factor 11 (GDF11) and myostatin (MSTN) are closely related TGFβ family members that are often believed to serve similar functions due to their high homology. However, genetic studies in animals provide clear evidence that they perform distinct roles. While the loss of
Mstn
leads to hypermuscularity, the deletion of
Gdf11
results in abnormal skeletal patterning and organ development. The perinatal lethality of
Gdf11
-null mice, which contrasts with the long-term viability of
Mstn
-null mice, has led most research to focus on utilizing recombinant GDF11 proteins to investigate the postnatal functions of GDF11. However, the reported outcomes of the exogenous application of recombinant GDF11 proteins are controversial partly because of the different sources and qualities of recombinant GDF11 used and because recombinant GDF11 and MSTN proteins are nearly indistinguishable due to their similar structural and biochemical properties. Here, we analyze the similarities and differences between GDF11 and MSTN from an evolutionary point of view and summarize the current understanding of the biological processing, signaling, and physiological functions of GDF11 and MSTN. Finally, we discuss the potential use of recombinant GDF11 as a therapeutic option for a wide range of medical conditions and the possible adverse effects of GDF11 inhibition mediated by MSTN inhibitors.
Growth factors: untangling twin proteins
A growth factor protein called GDF11 has potential for rejuvenation of heart, brain, and muscle tissues, but first its relationship with a twin growth factor (MSTN) must be unraveled. Although GDF11 and MSTN are almost identical in amino acid sequence, MSTN controls growth of skeletal muscles, and GDF11 regulates bone and organ patterning. To untangle what differentiates these proteins, Yun-Sil Lee and Joonho Suh at Seoul National University, South Korea, reviewed their evolution and function. They report that GDF11 and MSTN are the result of duplication of an original gene and have evolved to perform different roles. They cover some of the beneficial effects reported with GDF11 supplementation, such as tissue rejuvenation and increased lifespan, but caution that negative effects have been reported. Further investigation may illuminate growth and development processes, and therapeutic potential.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>33077875</pmid><doi>10.1038/s12276-020-00516-4</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0002-1228-0404</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 13 13/100 38 38/1 38/89 631/208/182 631/45/127/1219 631/80/86/2368 64 82 96 96/21 96/44 Amino acid sequence Biochemistry & Molecular Biology Biomedical and Life Sciences Biomedicine Growth differentiation factor 11 Growth factors Homology Information processing Lethality Life Sciences & Biomedicine Life span Medical Biochemistry Medicine, Research & Experimental Molecular Medicine Myostatin Pattern formation Proteins Research & Experimental Medicine Review Review Article Science & Technology Skeletal muscle Stem Cells Supplements 생화학 |
title | Similar sequences but dissimilar biological functions of GDF11 and myostatin |
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