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An exploration of the sequence of a 2.9-Mb region of the genome of Drosophila melanogaster: the Adh region.

机译:探索果蝇果蝇基因组2.9-Mb区域的序列:Adh区域。

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摘要

A contiguous sequence of nearly 3 Mb from the genome of Drosophila melanogaster has been sequenced from a series of overlapping P1 and BAC clones. This region covers 69 chromosome polytene bands on chromosome arm 2L, including the genetically well-characterized "Adh region." A computational analysis of the sequence predicts 218 protein-coding genes, 11 tRNAs, and 17 transposable element sequences. At least 38 of the protein-coding genes are arranged in clusters of from 2 to 6 closely related genes, suggesting extensive tandem duplication. The gene density is one protein-coding gene every 13 kb; the transposable element density is one element every 171 kb. Of 73 genes in this region identified by genetic analysis, 49 have been located on the sequence; P-element insertions have been mapped to 43 genes. Ninety-five (44%) of the known and predicted genes match a Drosophila EST, and 144 (66%) have clear similarities to proteins in other organisms. Genes known to have mutant phenotypes are more likely to be represented in cDNA libraries, and far more likely to have products similar to proteins of other organisms, than are genes with no known mutant phenotype. Over 650 chromosome aberration breakpoints map to this chromosome region, and their nonrandom distribution on the genetic map reflects variation in gene spacing on the DNA. This is the first large-scale analysis of the genome of D. melanogaster at the sequence level. In addition to the direct results obtained, this analysis has allowed us to develop and test methods that will be needed to interpret the complete sequence of the genome of this species.Before beginning a Hunt, it is wise to ask someone what you are looking for before you begin looking for it. Milne 1926
机译:已从一系列重叠的P1和BAC克隆中测序了来自果蝇果蝇(Drosophila melanogaster)基因组的近3 Mb的连续序列。该区域覆盖了第2L号染色体臂上的69条染色体多条带,其中包括遗传学特征明确的“ Adh区”。对该序列的计算分析可预测218个蛋白质编码基因,11个tRNA和17个可转座元件序列。至少38个蛋白质编码基因排列在2至6个紧密相关的基因簇中,表明广泛的串联重复。基因密度是每13 kb有一个蛋白质编码基因。转座子密度是每171 kb一个元素。通过遗传分析鉴定出该区域的73个基因中,有49个位于该序列上。 P元素插入已被映射到43个基因。 95%(44%)的已知和预测基因与果蝇EST匹配,而144(66%)的基因与其他生物中的蛋白质具有明显相似性。与没有已知突变表型的基因相比,已知具有突变表型的基因更有可能在cDNA文库中表达,并且更有可能具有与其他生物的蛋白质相似的产物。超过650个染色体畸变断点映射到该染色体区域,并且它们在遗传图谱上的非随机分布反映了DNA上基因间隔的变化。这是首次在序列水平上对黑腹果蝇的基因组进行大规模分析。除了获得直接的结果外,这项分析还使我们能够开发和测试解释该物种基因组完整序列所需的方法。开始狩猎之前,明智的做法是询问某人您正在寻找什么在您开始寻找之前。米尔恩1926

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