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幼虫和蛹前期发育期间果蝇唾液腺蛋白质的合成与分泌

Synthesis and secretion of salivary gland proteins in Drosophila gibberosa during larval and prepupal development.

作者信息

Shirk Paul David, Roberts Paul Alfred, Harn Chee Hark

机构信息

Insect Attractants, Behavior, and Basic Biology Research Laboratory, Agricultural Research Service, US Department of Agriculture, 32604, Gainesville, FL, USA.

Department of Zoology, Oregon State University, 97331, Corvallis, OR, USA.

出版信息

Rouxs Arch Dev Biol. 1988 Mar;197(2):66-74. doi: 10.1007/BF00375929.

DOI:10.1007/BF00375929
PMID:28305598
Abstract

The late larvae of Drosophila gibberosa Patterson and Mainland choose different pupariation sites than the larvae of Drosophila melanogaster Meigen. Since the larvae of D. gibberosa do not attach themselves to the substratum, the salivary glands contain only a small amount of the "glue" proteins before pupariation. Proteins comprising the salivary gland secretions of late larvae of these two species were compared and found to be qualitatively quite different. Only five polypeptides with the same molecular masses were identified in both species. The rate of protein synthesis in the salivary glands of D. gibberosa continued to increase through the late larval stage and pupariation. As a consequence, the total amount of protein contained in the salivary glands also continued to increase after pupariation. To demonstrate temporal changes in protein synthesis from 48 h before pupariation to 28 h after pupariation, newly synthesized polypeptides were pulse labeled by culturing salivary glands in vitro. The patterns of polypeptide synthesis fell into four major groups depending upon whether the synthesis of a protein stopped shortly after pupariation, stopped during late pupariation, increased at pupariation, or was initiated after pupariation. Changing patterns of protein synthesis are correlated with the known changes in gene puffing during this developmental period.

摘要

吉氏果蝇(Drosophila gibberosa Patterson和Mainland)的晚期幼虫与黑腹果蝇(Drosophila melanogaster Meigen)的幼虫选择不同的化蛹地点。由于吉氏果蝇的幼虫不会附着在基质上,其唾液腺在化蛹前仅含有少量的“胶水”蛋白。对这两个物种晚期幼虫唾液腺分泌物中的蛋白质进行了比较,发现它们在性质上有很大差异。在两个物种中仅鉴定出五种分子量相同的多肽。吉氏果蝇唾液腺中的蛋白质合成速率在幼虫晚期和化蛹过程中持续增加。因此,化蛹后唾液腺中所含蛋白质的总量也持续增加。为了证明从化蛹前48小时到化蛹后28小时蛋白质合成的时间变化,通过体外培养唾液腺对新合成的多肽进行脉冲标记。多肽合成模式分为四大类,这取决于蛋白质的合成在化蛹后不久是否停止、在化蛹后期停止、在化蛹时增加还是在化蛹后开始。蛋白质合成模式的变化与该发育时期已知的基因胀泡变化相关。

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本文引用的文献

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Patterns of protein synthesis in salivary glands ofDrosophila melanogaster during larval and prepupal development.黑腹果蝇幼虫和蛹前期发育过程中唾液腺的蛋白质合成模式。
Wilehm Roux Arch Dev Biol. 1981 Nov;190(6):351-357. doi: 10.1007/BF00863272.
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Synthesis and secretion of mucoprotein glue in the salivary gland ofDrosophila melanogaster.黑腹果蝇唾液腺中粘蛋白胶水的合成与分泌。
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Puffs and salivary gland function: The fine structure of the larval and prepupal salivary glands ofDrosophila melanogaster.
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An expandable gene that encodes a Drosophila glue protein is not expressed in variants lacking remote upstream sequences.一个编码果蝇胶水蛋白的可扩展基因在缺乏远端上游序列的变体中不表达。
Cell. 1982 Jul;29(3):1041-51. doi: 10.1016/0092-8674(82)90467-6.
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Cytogenetic and genetic mapping of a salivary gland secretion protein in Drosophila melanogaster.黑腹果蝇唾液腺分泌蛋白的细胞遗传学和基因定位
Chromosoma. 1981;84(2):173-85. doi: 10.1007/BF00399129.
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Molecular limits on the size of a genetic locus in Drosophila melanogaster.黑腹果蝇中一个基因座大小的分子限制
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7367-71. doi: 10.1073/pnas.77.12.7367.
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Molecular analysis of a gene in a developmentally regulated puff of Drosophila melanogaster.黑腹果蝇发育调控的唾腺染色体疏松区中一个基因的分子分析。
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