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一个用于研究全着丝粒害虫草地贪夜蛾的基因组BAC文库和一种新型BAC-GFP载体。

A genomic BAC library and a new BAC-GFP vector to study the holocentric pest Spodoptera frugiperda.

作者信息

d'Alençon Emmanuelle, Piffanelli Pietro, Volkoff Anne-Nathalie, Sabau Xavier, Gimenez Sylvie, Rocher Janick, Cérutti Pierre, Fournier Philippe

机构信息

Laboratoire de Pathologie Comparée, Institut National de la Recherche Agronomique (INRA) UMR 1231, Centre National de la recherche Scientifique (CNRS) FRE 2689, Univ. Montpellier II, 30380 Saint Christol-les-Alès, France.

出版信息

Insect Biochem Mol Biol. 2004 Apr;34(4):331-41. doi: 10.1016/j.ibmb.2003.12.004.

Abstract

Two genomic tools for the study of Lepidoptera and the holocentric structure of their chromosomes are presented in this paper. A bacterial artificial chromosome (BAC) library was constructed using nuclear DNA partially digested with HindIII from eggs of Spodoptera frugiperda. The library contains a total of 36,864 clones with an average insert size of 125 kb, which corresponds to approximately 11.5 genome equivalents. Hybridization screening of the library was performed with eight single-copy genes, giving an average hit of 10 clones per marker gene. Colinearity between the genome and BACs was demonstrated at the triose phosphate isomerase (tpi) locus. Probing of the library with a PCR fragment internal to the 18S ribosomal gene allowed an estimation of the rDNA locus size close to 115 repeats per haploid genome. A new vector (pBAC3.6eGFP) for transient transfection into S. frugiperda cell lines has been constructed. It is based on the BAC vector, pBAC3.6e, in which a gene encoding GFP was inserted under the control of the densovirus P9 promoter. This vector has the advantage to accommodate large genomic inserts and to be transfected in a large lepidopteran host range. It was used to construct a second BAC library from Sf9 cell nuclear DNA in order to allow a comparison between somatic and cell line genome organization.

摘要

本文介绍了两种用于研究鳞翅目及其染色体着丝粒结构的基因组工具。利用斜纹夜蛾卵中经HindIII部分消化的核DNA构建了一个细菌人工染色体(BAC)文库。该文库共包含36,864个克隆,平均插入片段大小为125 kb,约相当于11.5个基因组当量。用8个单拷贝基因对该文库进行杂交筛选,每个标记基因平均命中10个克隆。在磷酸丙糖异构酶(tpi)基因座处证明了基因组与BAC之间的共线性。用18S核糖体基因内部的PCR片段对文库进行探测,估计每个单倍体基因组的rDNA基因座大小接近115个重复序列。构建了一种用于瞬时转染斜纹夜蛾细胞系的新型载体(pBAC3.6eGFP)。它基于BAC载体pBAC3.6e,其中在浓核病毒P9启动子的控制下插入了一个编码绿色荧光蛋白的基因。该载体的优点是能够容纳大的基因组插入片段,并能在较大的鳞翅目宿主范围内进行转染。为了比较体细胞基因组和细胞系基因组的组织情况,用它从Sf9细胞核DNA构建了第二个BAC文库。

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