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波氏块菌菌丝体和子实体中差异表达基因的分离与鉴定

Isolation and characterization of differentially expressed genes in the mycelium and fruit body of Tuber borchii.

作者信息

Lacourt Isabelle, Duplessis Sébastien, Abbà Simona, Bonfante Paola, Martin Francis

机构信息

Dipartimento di Biologia Vegetale, Università di Torino and Sezione di Torino, Istituto di Protezione delle Piante-CNR, 10125 Turin, Italy.

出版信息

Appl Environ Microbiol. 2002 Sep;68(9):4574-82. doi: 10.1128/AEM.68.9.4574-4582.2002.

Abstract

The transition from vegetative mycelium to fruit body in truffles requires differentiation processes which lead to edible fruit bodies (ascomata) consisting of different cell and tissue types. The identification of genes differentially expressed during these developmental processes can contribute greatly to a better understanding of truffle morphogenesis. A cDNA library was constructed from vegetative mycelium RNAs of the white truffle Tuber borchii, and 214 cDNAs were sequenced. Up to 58% of the expressed sequence tags corresponded to known genes. The majority of the identified sequences represented housekeeping proteins, i.e., proteins involved in gene or protein expression, cell wall formation, primary and secondary metabolism, and signaling pathways. We screened 171 arrayed cDNAs by using cDNA probes constructed from mRNAs of vegetative mycelium and ascomata to identify fruit body-regulated genes. Comparisons of signals from vegetative mycelium and fruit bodies bearing 15 or 70% mature spores revealed significant differences in the expression levels for up to 33% of the investigated genes. The expression levels for six highly regulated genes were confirmed by RNA blot analyses. The expression of glutamine synthetase, 5-aminolevulinic acid synthetase, isocitrate lyase, thioredoxin, glucan 1,3-beta-glucosidase, and UDP-glucose:sterol glucosyl transferase was highly up-regulated, suggesting that amino acid biosynthesis, the glyoxylate cycle pathway, and cell wall synthesis are strikingly altered during morphogenesis.

摘要

松露从营养菌丝体向子实体的转变需要分化过程,这些过程会产生由不同细胞和组织类型组成的可食用子实体(子囊果)。鉴定在这些发育过程中差异表达的基因,对于更好地理解松露形态发生有很大帮助。从白松露(Tuber borchii)的营养菌丝体RNA构建了一个cDNA文库,并对214个cDNA进行了测序。高达58%的表达序列标签对应于已知基因。大多数鉴定出的序列代表管家蛋白,即参与基因或蛋白质表达、细胞壁形成、初级和次级代谢以及信号通路的蛋白质。我们使用从营养菌丝体和子囊果的mRNA构建的cDNA探针,筛选了171个排列好的cDNA,以鉴定受子实体调控的基因。比较来自营养菌丝体和带有15%或70%成熟孢子的子实体的信号,发现高达33%的被研究基因的表达水平存在显著差异。通过RNA印迹分析证实了六个高度调控基因的表达水平。谷氨酰胺合成酶、5-氨基乙酰丙酸合成酶、异柠檬酸裂合酶、硫氧还蛋白、葡聚糖1,3-β-葡萄糖苷酶和UDP-葡萄糖:甾醇葡萄糖基转移酶的表达高度上调,表明在形态发生过程中氨基酸生物合成、乙醛酸循环途径和细胞壁合成发生了显著变化。

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