Transcriptomic, proteomic, and metabolomic landscape of positional memory in the caudal fin of zebrafish
Regeneration requires cells to regulate proliferation and patterning according to their spatial position. Positional memory is a property that enables regenerating cells to recall spatial information from the uninjured tissue. Positional memory is hypothesized to rely on gradients of molecules, few...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2017-01, Vol.114 (5), p.E717-E726 |
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creator | Rabinowitz, Jeremy S. Robitaille, Aaron M. Wang, Yuliang Ray, Catherine A. Thummel, Ryan Gu, Haiwei Djukovic, Danijel Raftery, Daniel Berndt, Jason D. Moon, Randall T. |
description | Regeneration requires cells to regulate proliferation and patterning according to their spatial position. Positional memory is a property that enables regenerating cells to recall spatial information from the uninjured tissue. Positional memory is hypothesized to rely on gradients of molecules, few of which have been identified. Here, we quantified the global abundance of transcripts, proteins, and metabolites along the proximodistal axis of caudal fins of uninjured and regenerating adult zebrafish. Using this approach, we uncovered complex overlapping expression patterns for hundreds of molecules involved in diverse cellular functions, including development, bioelectric signaling, and amino acid and lipid metabolism. Moreover, 32 genes differentially expressed at the RNA level had concomitant differential expression of the encoded proteins. Thus, the identification of proximodistal differences in levels of RNAs, proteins, and metabolites will facilitate future functional studies of positional memory during appendage regeneration. |
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Positional memory is a property that enables regenerating cells to recall spatial information from the uninjured tissue. Positional memory is hypothesized to rely on gradients of molecules, few of which have been identified. Here, we quantified the global abundance of transcripts, proteins, and metabolites along the proximodistal axis of caudal fins of uninjured and regenerating adult zebrafish. Using this approach, we uncovered complex overlapping expression patterns for hundreds of molecules involved in diverse cellular functions, including development, bioelectric signaling, and amino acid and lipid metabolism. Moreover, 32 genes differentially expressed at the RNA level had concomitant differential expression of the encoded proteins. Thus, the identification of proximodistal differences in levels of RNAs, proteins, and metabolites will facilitate future functional studies of positional memory during appendage regeneration.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.1620755114</identifier><identifier>PMID: 28096348</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Biological Sciences ; Cells ; Danio rerio ; Memory ; Metabolites ; Molecules ; PNAS Plus ; Proteins ; Recall</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2017-01, Vol.114 (5), p.E717-E726</ispartof><rights>Volumes 1–89 and 106–114, copyright as a collective work only; author(s) retains copyright to individual articles</rights><rights>Copyright National Academy of Sciences Jan 31, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c542t-fc7fdd907e15796da7894dcafd4f33bcc1bbc1460de6f8e5a13f1721638e6f7a3</citedby><cites>FETCH-LOGICAL-c542t-fc7fdd907e15796da7894dcafd4f33bcc1bbc1460de6f8e5a13f1721638e6f7a3</cites><orcidid>0000-0002-6981-6863</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/26479169$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/26479169$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28096348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rabinowitz, Jeremy S.</creatorcontrib><creatorcontrib>Robitaille, Aaron M.</creatorcontrib><creatorcontrib>Wang, Yuliang</creatorcontrib><creatorcontrib>Ray, Catherine A.</creatorcontrib><creatorcontrib>Thummel, Ryan</creatorcontrib><creatorcontrib>Gu, Haiwei</creatorcontrib><creatorcontrib>Djukovic, Danijel</creatorcontrib><creatorcontrib>Raftery, Daniel</creatorcontrib><creatorcontrib>Berndt, Jason D.</creatorcontrib><creatorcontrib>Moon, Randall T.</creatorcontrib><title>Transcriptomic, proteomic, and metabolomic landscape of positional memory in the caudal fin of zebrafish</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Regeneration requires cells to regulate proliferation and patterning according to their spatial position. Positional memory is a property that enables regenerating cells to recall spatial information from the uninjured tissue. Positional memory is hypothesized to rely on gradients of molecules, few of which have been identified. Here, we quantified the global abundance of transcripts, proteins, and metabolites along the proximodistal axis of caudal fins of uninjured and regenerating adult zebrafish. Using this approach, we uncovered complex overlapping expression patterns for hundreds of molecules involved in diverse cellular functions, including development, bioelectric signaling, and amino acid and lipid metabolism. Moreover, 32 genes differentially expressed at the RNA level had concomitant differential expression of the encoded proteins. Thus, the identification of proximodistal differences in levels of RNAs, proteins, and metabolites will facilitate future functional studies of positional memory during appendage regeneration.</description><subject>Biological Sciences</subject><subject>Cells</subject><subject>Danio rerio</subject><subject>Memory</subject><subject>Metabolites</subject><subject>Molecules</subject><subject>PNAS Plus</subject><subject>Proteins</subject><subject>Recall</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkUtv1TAQhS0EopfCmhUoUjcsSOuJ3xukquJRqRKbsrYcP7i-SuJgJ5XKr8eXW1roipXtM5-PZuYg9BrwKWBBzubJlFPgHRaMAdAnaANYQcupwk_RBuNOtJJ29Ai9KGWHMVZM4ufoqJNYcULlBm2vs5mKzXFe0hjt-2bOafGHq5lcM_rF9GnYC81QhWLN7JsUmjmVuMQ0maEyY8q3TZyaZesba1ZXxVCfFfvp-2xCLNuX6FkwQ_Gv7s5j9O3Tx-uLL-3V18-XF-dXrWW0W9pgRXBOYeGBCcWdEVJRZ01wNBDSWwt9b4Fy7DwP0jMDJIDogBNZBWHIMfpw8J3XfvTO-mnJZtBzjqPJtzqZqP-tTHGrv6cbzTpF6gqrwbs7g5x-rL4seozF-qFO79NaNEgJggtB5X-gHBin0O1dTx6hu7Tmur3fFGO4w5hU6uxA2ZxKyT7c9w1Y7wPX-8D1Q-D1x9u_x73n_yRcgTcHYFeWlB_qnAoFXJFfc96y2A</recordid><startdate>20170131</startdate><enddate>20170131</enddate><creator>Rabinowitz, Jeremy S.</creator><creator>Robitaille, Aaron M.</creator><creator>Wang, Yuliang</creator><creator>Ray, Catherine A.</creator><creator>Thummel, Ryan</creator><creator>Gu, Haiwei</creator><creator>Djukovic, Danijel</creator><creator>Raftery, Daniel</creator><creator>Berndt, Jason D.</creator><creator>Moon, Randall T.</creator><general>National Academy of Sciences</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</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><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6981-6863</orcidid></search><sort><creationdate>20170131</creationdate><title>Transcriptomic, proteomic, and metabolomic landscape of positional memory in the caudal fin of zebrafish</title><author>Rabinowitz, Jeremy S. ; 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subjects | Biological Sciences Cells Danio rerio Memory Metabolites Molecules PNAS Plus Proteins Recall |
title | Transcriptomic, proteomic, and metabolomic landscape of positional memory in the caudal fin of zebrafish |
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