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本文引用的文献

1
Tissue-specific DNase l-sensitive sites of the maize P gene and their changes upon epimutation.玉米P基因的组织特异性脱氧核糖核酸酶I敏感位点及其在表观突变后的变化。
Plant J. 1995 May;7(5):797-807.
2
Whole-genome validation of high-information-content fingerprinting.高信息含量指纹图谱的全基因组验证
Plant Physiol. 2005 Sep;139(1):27-38. doi: 10.1104/pp.105.061978.
3
The map-based sequence of the rice genome.水稻基因组的基于图谱的序列。
Nature. 2005 Aug 11;436(7052):793-800. doi: 10.1038/nature03895.
4
Gene movement by Helitron transposons contributes to the haplotype variability of maize.Helitron转座子介导的基因移动有助于玉米单倍型的多样性。
Proc Natl Acad Sci U S A. 2005 Jun 21;102(25):9068-73. doi: 10.1073/pnas.0502923102. Epub 2005 Jun 10.
5
Sorghum genome sequencing by methylation filtration.通过甲基化过滤进行高粱基因组测序。
PLoS Biol. 2005 Jan;3(1):e13. doi: 10.1371/journal.pbio.0030013. Epub 2005 Jan 4.
6
Evolution of DNA sequence nonhomologies among maize inbreds.玉米自交系间DNA序列非同源性的进化
Plant Cell. 2005 Feb;17(2):343-60. doi: 10.1105/tpc.104.025627. Epub 2005 Jan 19.
7
Characterization of the maize endosperm transcriptome and its comparison to the rice genome.玉米胚乳转录组的特征分析及其与水稻基因组的比较。
Genome Res. 2004 Oct;14(10A):1932-7. doi: 10.1101/gr.2780504.
8
Gene loss and movement in the maize genome.玉米基因组中的基因丢失与转移
Genome Res. 2004 Oct;14(10A):1924-31. doi: 10.1101/gr.2701104.
9
Close split of sorghum and maize genome progenitors.高粱和玉米基因组祖先的紧密分化
Genome Res. 2004 Oct;14(10A):1916-23. doi: 10.1101/gr.2332504.
10
Sequence composition and genome organization of maize.玉米的序列组成与基因组结构
Proc Natl Acad Sci U S A. 2004 Oct 5;101(40):14349-54. doi: 10.1073/pnas.0406163101. Epub 2004 Sep 23.

玉米基因组的结构与架构。

Structure and architecture of the maize genome.

作者信息

Haberer Georg, Young Sarah, Bharti Arvind K, Gundlach Heidrun, Raymond Christina, Fuks Galina, Butler Ed, Wing Rod A, Rounsley Steve, Birren Bruce, Nusbaum Chad, Mayer Klaus F X, Messing Joachim

机构信息

Munich Information Center for Protein Sequences, Institute for Bioinformatics, Gesellschaft für Strahlenforschung Research Center for Environment and Health, D-85764 Neuherberg, Germany.

出版信息

Plant Physiol. 2005 Dec;139(4):1612-24. doi: 10.1104/pp.105.068718.

DOI:10.1104/pp.105.068718
PMID:16339807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1310546/
Abstract

Maize (Zea mays or corn) plays many varied and important roles in society. It is not only an important experimental model plant, but also a major livestock feed crop and a significant source of industrial products such as sweeteners and ethanol. In this study we report the systematic analysis of contiguous sequences of the maize genome. We selected 100 random regions averaging 144 kb in size, representing about 0.6% of the genome, and generated a high-quality dataset for sequence analysis. This sampling contains 330 annotated genes, 91% of which are supported by expressed sequence tag data from maize and other cereal species. Genes averaged 4 kb in size with five exons, although the largest was over 59 kb with 31 exons. Gene density varied over a wide range from 0.5 to 10.7 genes per 100 kb and genes did not appear to cluster significantly. The total repetitive element content we observed (66%) was slightly higher than previous whole-genome estimates (58%-63%) and consisted almost exclusively of retroelements. The vast majority of genes can be aligned to at least one sequence read derived from gene-enrichment procedures, but only about 30% are fully covered. Our results indicate that much of the increase in genome size of maize relative to rice (Oryza sativa) and Arabidopsis (Arabidopsis thaliana) is attributable to an increase in number of both repetitive elements and genes.

摘要

玉米(Zea mays 或corn)在社会中扮演着多种重要角色。它不仅是一种重要的实验模式植物,还是主要的家畜饲料作物,以及甜味剂和乙醇等工业产品的重要来源。在本研究中,我们报告了对玉米基因组连续序列的系统分析。我们随机选择了100个平均大小为144 kb的区域,约占基因组的0.6%,并生成了用于序列分析的高质量数据集。该样本包含330个注释基因,其中91%得到了来自玉米和其他谷类物种的表达序列标签数据的支持。基因平均大小为4 kb,有五个外显子,尽管最大的基因超过59 kb,有31个外显子。基因密度在每100 kb 0.5至10.7个基因的广泛范围内变化,且基因似乎没有明显的聚集现象。我们观察到的总重复元件含量(66%)略高于先前的全基因组估计值(58%-63%),且几乎全部由反转录元件组成。绝大多数基因可以与至少一个来自基因富集程序的序列读数比对,但只有约30%被完全覆盖。我们的结果表明,相对于水稻(Oryza sativa)和拟南芥(Arabidopsis thaliana),玉米基因组大小的增加很大程度上归因于重复元件和基因数量的增加。