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利用果蝇睾丸转录的计算分析和微阵列分析进行基因发现。

Gene discovery using computational and microarray analysis of transcription in the Drosophila melanogaster testis.

作者信息

Andrews J, Bouffard G G, Cheadle C, Lü J, Becker K G, Oliver B

机构信息

Laboratory of Cellular and Developmental Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Genome Res. 2000 Dec;10(12):2030-43. doi: 10.1101/gr.10.12.2030.

Abstract

Identification and annotation of all the genes in the sequenced Drosophila genome is a work in progress. Wild-type testis function requires many genes and is thus of potentially high value for the identification of transcription units. We therefore undertook a survey of the repertoire of genes expressed in the Drosophila testis by computational and microarray analysis. We generated 3141 high-quality testis expressed sequence tags (ESTs). Testis ESTs computationally collapsed into 1560 cDNA set used for further analysis. Of those, 11% correspond to named genes, and 33% provide biological evidence for a predicted gene. A surprising 47% fail to align with existing ESTs and 16% with predicted genes in the current genome release. EST frequency and microarray expression profiles indicate that the testis mRNA population is highly complex and shows an extended range of transcript abundance. Furthermore, >80% of the genes expressed in the testis showed onefold overexpression relative to ovaries, or gonadectomized flies. Additionally, >3% showed more than threefold overexpression at p <0.05. Surprisingly, 22% of the genes most highly overexpressed in testis match Drosophila genomic sequence, but not predicted genes. These data strongly support the idea that sequencing additional cDNA libraries from defined tissues, such as testis, will be important tools for refined annotation of the Drosophila genome. Additionally, these data suggest that the number of genes in Drosophila will significantly exceed the conservative estimate of 13,601.

摘要

对已测序的果蝇基因组中的所有基因进行识别和注释工作仍在进行中。野生型睾丸功能需要许多基因,因此对于转录单位的识别具有潜在的高价值。我们因此通过计算和微阵列分析对果蝇睾丸中表达的基因库进行了一项调查。我们生成了3141个高质量的睾丸表达序列标签(EST)。通过计算将睾丸EST归并为1560个cDNA集用于进一步分析。其中,11%对应于已命名的基因,33%为预测基因提供了生物学证据。令人惊讶的是,47%未能与现有EST对齐,16%未能与当前基因组版本中的预测基因对齐。EST频率和微阵列表达谱表明,睾丸mRNA群体高度复杂,转录本丰度范围广泛。此外,在睾丸中表达的基因中有超过80%相对于卵巢或去性腺果蝇表现出一倍的过表达。此外,在p<0.05时,超过3%表现出超过三倍的过表达。令人惊讶的是,在睾丸中过表达程度最高的基因中有22%与果蝇基因组序列匹配,但与预测基因不匹配。这些数据有力地支持了这样一种观点,即从特定组织(如睾丸)测序额外的cDNA文库将是完善果蝇基因组注释的重要工具。此外,这些数据表明果蝇中的基因数量将显著超过13601这个保守估计数。

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