Crystalline yolk spheroids in Drosophila melanogaster oocyte: Freeze fracture and two-dimensional reconstruction analysis
The major sites of energy storage during oogenesis in the Drosophila melanogaster oocyte are the α- and β-yolk spheres. By applying biochemical and transmission electron microscopy (TEM) immunogold techniques we found that the β-yolk spheres contain mainly polysaccharides, while the three main yolk...
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Veröffentlicht in: | Journal of insect physiology 2007-04, Vol.53 (4), p.370-376 |
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creator | Papassideri, Issidora S. Trougakos, Ioannis P. Leonard, Kevin R. Margaritis, Lukas H. |
description | The major sites of energy storage during oogenesis in the
Drosophila melanogaster oocyte are the
α- and
β-yolk spheres. By applying biochemical and transmission electron microscopy (TEM) immunogold techniques we found that the
β-yolk spheres contain mainly polysaccharides, while the three main yolk proteins (YPs) are stored in the
α-yolk spheres of the developing oocyte. Moreover, by using high-resolution TEM of freeze fractured or cryosectioned follicles, we identified the existence of crystalline structures within the
α-yolk spheres of the mature oocyte. Our subsequent two-dimensional reconstruction analysis revealed that the unit cell of the crystal is about 113
Å×113
Å. Assuming that the repeating unit is a cylinder of about 110
Å in length and 25
Å in diameter this cylinder would then have a volume of about 50,000
cubic
Å, which corresponds to about 40
kDa of protein. This size fits quite well with the known molecular weight of about 40–45
kDa for each of the three
D. melanogaster YPs. Overall, our study identifies for the first time the supramolecular arrangement of the
α-yolk spheres constituent molecules and provides direct evidence for the “natural” crystallization, and therefore the efficient packaging, of the YPs during oogenesis. |
doi_str_mv | 10.1016/j.jinsphys.2006.12.011 |
format | Article |
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Drosophila melanogaster oocyte are the
α- and
β-yolk spheres. By applying biochemical and transmission electron microscopy (TEM) immunogold techniques we found that the
β-yolk spheres contain mainly polysaccharides, while the three main yolk proteins (YPs) are stored in the
α-yolk spheres of the developing oocyte. Moreover, by using high-resolution TEM of freeze fractured or cryosectioned follicles, we identified the existence of crystalline structures within the
α-yolk spheres of the mature oocyte. Our subsequent two-dimensional reconstruction analysis revealed that the unit cell of the crystal is about 113
Å×113
Å. Assuming that the repeating unit is a cylinder of about 110
Å in length and 25
Å in diameter this cylinder would then have a volume of about 50,000
cubic
Å, which corresponds to about 40
kDa of protein. This size fits quite well with the known molecular weight of about 40–45
kDa for each of the three
D. melanogaster YPs. Overall, our study identifies for the first time the supramolecular arrangement of the
α-yolk spheres constituent molecules and provides direct evidence for the “natural” crystallization, and therefore the efficient packaging, of the YPs during oogenesis.</description><identifier>ISSN: 0022-1910</identifier><identifier>EISSN: 1879-1611</identifier><identifier>DOI: 10.1016/j.jinsphys.2006.12.011</identifier><identifier>PMID: 17292389</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>2-D reconstruction ; analytical methods ; Animals ; computer analysis ; Cryo-immunocytochemistry ; crystal structure ; Crystalline yolk ; Drosophila melanogaster ; Egg Proteins - metabolism ; egg yolk ; Egg Yolk - ultrastructure ; Female ; Freeze fracture ; Freeze Fracturing ; Image Processing, Computer-Assisted ; immunocytochemistry ; In situ sugar detection ; Microscopy, Electron, Transmission ; Oocyte ; oocytes ; Oocytes - ultrastructure ; yolk proteins</subject><ispartof>Journal of insect physiology, 2007-04, Vol.53 (4), p.370-376</ispartof><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-e387eea87045eb03450ae5ff7b5a238466ca333a43efa5caaa8547f95da70d023</citedby><cites>FETCH-LOGICAL-c421t-e387eea87045eb03450ae5ff7b5a238466ca333a43efa5caaa8547f95da70d023</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jinsphys.2006.12.011$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17292389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Papassideri, Issidora S.</creatorcontrib><creatorcontrib>Trougakos, Ioannis P.</creatorcontrib><creatorcontrib>Leonard, Kevin R.</creatorcontrib><creatorcontrib>Margaritis, Lukas H.</creatorcontrib><title>Crystalline yolk spheroids in Drosophila melanogaster oocyte: Freeze fracture and two-dimensional reconstruction analysis</title><title>Journal of insect physiology</title><addtitle>J Insect Physiol</addtitle><description>The major sites of energy storage during oogenesis in the
Drosophila melanogaster oocyte are the
α- and
β-yolk spheres. By applying biochemical and transmission electron microscopy (TEM) immunogold techniques we found that the
β-yolk spheres contain mainly polysaccharides, while the three main yolk proteins (YPs) are stored in the
α-yolk spheres of the developing oocyte. Moreover, by using high-resolution TEM of freeze fractured or cryosectioned follicles, we identified the existence of crystalline structures within the
α-yolk spheres of the mature oocyte. Our subsequent two-dimensional reconstruction analysis revealed that the unit cell of the crystal is about 113
Å×113
Å. Assuming that the repeating unit is a cylinder of about 110
Å in length and 25
Å in diameter this cylinder would then have a volume of about 50,000
cubic
Å, which corresponds to about 40
kDa of protein. This size fits quite well with the known molecular weight of about 40–45
kDa for each of the three
D. melanogaster YPs. Overall, our study identifies for the first time the supramolecular arrangement of the
α-yolk spheres constituent molecules and provides direct evidence for the “natural” crystallization, and therefore the efficient packaging, of the YPs during oogenesis.</description><subject>2-D reconstruction</subject><subject>analytical methods</subject><subject>Animals</subject><subject>computer analysis</subject><subject>Cryo-immunocytochemistry</subject><subject>crystal structure</subject><subject>Crystalline yolk</subject><subject>Drosophila melanogaster</subject><subject>Egg Proteins - metabolism</subject><subject>egg yolk</subject><subject>Egg Yolk - ultrastructure</subject><subject>Female</subject><subject>Freeze fracture</subject><subject>Freeze Fracturing</subject><subject>Image Processing, Computer-Assisted</subject><subject>immunocytochemistry</subject><subject>In situ sugar detection</subject><subject>Microscopy, Electron, Transmission</subject><subject>Oocyte</subject><subject>oocytes</subject><subject>Oocytes - ultrastructure</subject><subject>yolk proteins</subject><issn>0022-1910</issn><issn>1879-1611</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS0EokvhKxSfuCXMJHH-cAItFJAqcYCerVln0npJ4sV2qMKnx6tdxLGnkUa_eTPznhBXCDkC1m_3-d7O4XC_hrwAqHMsckB8IjbYNl2GNeJTsQEoigw7hAvxIoQ9AKi6Vc_FBTZFV5RttxHr1q8h0jjameXqxp8yibJ3tg_SzvKjd8Ed7u1IcuKRZndHIbKXzpk18jt57Zn_sBw8mbh4ljT3Mj64rLcTz8G6mUbp2bg5RL-YmBoJoXENNrwUzwYaA78610txe_3px_ZLdvPt89fth5vMVAXGjMu2Yaa2gUrxDspKAbEahmanKL1Q1bWhsiypKnkgZYioVVUzdKqnBnooykvx5qR78O7XwiHqyQbDY_qG3RJ0kzSxU9WjIHZ13QF2CaxPoEnuBM-DPng7kV81gj6mo_f6Xzr6mI7GQqd00uDVecOym7j_P3aOIwGvT8BATtOdt0Hffi8AS4DmuFwl4v2J4GTZb8teB2N5Ntzb5HPUvbOPXfEXFjOxVA</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Papassideri, Issidora S.</creator><creator>Trougakos, Ioannis P.</creator><creator>Leonard, Kevin R.</creator><creator>Margaritis, Lukas H.</creator><general>Elsevier 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>7SS</scope><scope>7X8</scope></search><sort><creationdate>20070401</creationdate><title>Crystalline yolk spheroids in Drosophila melanogaster oocyte: Freeze fracture and two-dimensional reconstruction analysis</title><author>Papassideri, Issidora S. ; Trougakos, Ioannis P. ; Leonard, Kevin R. ; Margaritis, Lukas H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-e387eea87045eb03450ae5ff7b5a238466ca333a43efa5caaa8547f95da70d023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>2-D reconstruction</topic><topic>analytical methods</topic><topic>Animals</topic><topic>computer analysis</topic><topic>Cryo-immunocytochemistry</topic><topic>crystal structure</topic><topic>Crystalline yolk</topic><topic>Drosophila melanogaster</topic><topic>Egg Proteins - metabolism</topic><topic>egg yolk</topic><topic>Egg Yolk - ultrastructure</topic><topic>Female</topic><topic>Freeze fracture</topic><topic>Freeze Fracturing</topic><topic>Image Processing, Computer-Assisted</topic><topic>immunocytochemistry</topic><topic>In situ sugar detection</topic><topic>Microscopy, Electron, Transmission</topic><topic>Oocyte</topic><topic>oocytes</topic><topic>Oocytes - ultrastructure</topic><topic>yolk proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Papassideri, Issidora S.</creatorcontrib><creatorcontrib>Trougakos, Ioannis P.</creatorcontrib><creatorcontrib>Leonard, Kevin R.</creatorcontrib><creatorcontrib>Margaritis, Lukas H.</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>Entomology Abstracts (Full archive)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of insect physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Papassideri, Issidora S.</au><au>Trougakos, Ioannis P.</au><au>Leonard, Kevin R.</au><au>Margaritis, Lukas H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Crystalline yolk spheroids in Drosophila melanogaster oocyte: Freeze fracture and two-dimensional reconstruction analysis</atitle><jtitle>Journal of insect physiology</jtitle><addtitle>J Insect Physiol</addtitle><date>2007-04-01</date><risdate>2007</risdate><volume>53</volume><issue>4</issue><spage>370</spage><epage>376</epage><pages>370-376</pages><issn>0022-1910</issn><eissn>1879-1611</eissn><abstract>The major sites of energy storage during oogenesis in the
Drosophila melanogaster oocyte are the
α- and
β-yolk spheres. By applying biochemical and transmission electron microscopy (TEM) immunogold techniques we found that the
β-yolk spheres contain mainly polysaccharides, while the three main yolk proteins (YPs) are stored in the
α-yolk spheres of the developing oocyte. Moreover, by using high-resolution TEM of freeze fractured or cryosectioned follicles, we identified the existence of crystalline structures within the
α-yolk spheres of the mature oocyte. Our subsequent two-dimensional reconstruction analysis revealed that the unit cell of the crystal is about 113
Å×113
Å. Assuming that the repeating unit is a cylinder of about 110
Å in length and 25
Å in diameter this cylinder would then have a volume of about 50,000
cubic
Å, which corresponds to about 40
kDa of protein. This size fits quite well with the known molecular weight of about 40–45
kDa for each of the three
D. melanogaster YPs. Overall, our study identifies for the first time the supramolecular arrangement of the
α-yolk spheres constituent molecules and provides direct evidence for the “natural” crystallization, and therefore the efficient packaging, of the YPs during oogenesis.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>17292389</pmid><doi>10.1016/j.jinsphys.2006.12.011</doi><tpages>7</tpages></addata></record> |
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subjects | 2-D reconstruction analytical methods Animals computer analysis Cryo-immunocytochemistry crystal structure Crystalline yolk Drosophila melanogaster Egg Proteins - metabolism egg yolk Egg Yolk - ultrastructure Female Freeze fracture Freeze Fracturing Image Processing, Computer-Assisted immunocytochemistry In situ sugar detection Microscopy, Electron, Transmission Oocyte oocytes Oocytes - ultrastructure yolk proteins |
title | Crystalline yolk spheroids in Drosophila melanogaster oocyte: Freeze fracture and two-dimensional reconstruction analysis |
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