The size and sequence organization of the centromeric region of Arabidopsis thaliana chromosome 4.

N. Kumekawa, T. Hosouchi, H. Tsuruoka, Hirokazu Kotani
{"title":"The size and sequence organization of the centromeric region of Arabidopsis thaliana chromosome 4.","authors":"N. Kumekawa, T. Hosouchi, H. Tsuruoka, Hirokazu Kotani","doi":"10.1093/DNARES/8.6.285","DOIUrl":null,"url":null,"abstract":"We have determined the genome structure of the centromeric region of Arabidopsis thaliana chromosome 4 by sequence analysis of BAC clones obtained by genome walking, followed by construction of a physical map using DNA of a hypomethylated strain. The total size of the centromeric region, corresponding to the recombinant inbred (RI) markers between mi87 and mi167, was approximately 5.3 megabases (Mb). This value is over 3 Mb longer than that previously estimated by the Arabidopsis Genome Initiative (Nature, 408, 796-815, 2000). Although we could not cover the entire centromeric region by BAC clones because of the presence of highly repetitive sequences in the middle (2.7 Mb), the cloned regions spanning approximately 1 Mb at both sides of the gap were newly sequenced. These results together with the reported sequences in the adjacent regions suggest that the centromeric region is principally composed of a central domain of 2.7 Mb, consisting of mainly 180-bp repeats and Athila elements, and upper and lower flanking regions of 1.55 Mb and 1 Mb, respectively. The flanking regions were predominantly composed of various types of transposable elements, except for the upper end moiety in which a large 5S rDNA array (0.65 Mb) and central domain-like sequence are present. Such an organization is essentially identical to the centromeric region of chromosome 5 reported previously.","PeriodicalId":11212,"journal":{"name":"DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes","volume":"2007 1","pages":"285-90"},"PeriodicalIF":0.0000,"publicationDate":"2001-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"105","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/DNARES/8.6.285","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 105

Abstract

We have determined the genome structure of the centromeric region of Arabidopsis thaliana chromosome 4 by sequence analysis of BAC clones obtained by genome walking, followed by construction of a physical map using DNA of a hypomethylated strain. The total size of the centromeric region, corresponding to the recombinant inbred (RI) markers between mi87 and mi167, was approximately 5.3 megabases (Mb). This value is over 3 Mb longer than that previously estimated by the Arabidopsis Genome Initiative (Nature, 408, 796-815, 2000). Although we could not cover the entire centromeric region by BAC clones because of the presence of highly repetitive sequences in the middle (2.7 Mb), the cloned regions spanning approximately 1 Mb at both sides of the gap were newly sequenced. These results together with the reported sequences in the adjacent regions suggest that the centromeric region is principally composed of a central domain of 2.7 Mb, consisting of mainly 180-bp repeats and Athila elements, and upper and lower flanking regions of 1.55 Mb and 1 Mb, respectively. The flanking regions were predominantly composed of various types of transposable elements, except for the upper end moiety in which a large 5S rDNA array (0.65 Mb) and central domain-like sequence are present. Such an organization is essentially identical to the centromeric region of chromosome 5 reported previously.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
拟南芥4号染色体着丝区大小和序列组织。
我们通过基因组行走获得的BAC克隆序列分析,确定了拟南芥4号染色体着丝粒区域的基因组结构,然后利用低甲基化菌株的DNA构建了物理图谱。与mi87和mi167之间的重组自交系(RI)标记相对应的着丝粒区总大小约为5.3兆碱基(Mb)。这个值比拟南芥基因组计划(Nature, 408, 796-815, 2000)先前估计的要长3mb以上。虽然我们不能用BAC克隆覆盖整个着丝粒区,因为在中间(2.7 Mb)存在高度重复的序列,但在间隔两侧大约1mb的克隆区域都是新测序的。这些结果和邻近区域的序列表明,着丝粒区主要由2.7 Mb的中心区域和1.55 Mb的上下侧翼区域组成,中心区域主要由180-bp的重复序列和Athila元件组成。侧翼区主要由各种类型的转座元件组成,除了上部部分存在较大的5S rDNA阵列(0.65 Mb)和中心结构域序列。这种组织本质上与先前报道的5号染色体的着丝粒区域相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Telomere-to-telomere genome assembly of Oldenlandia diffusa Genome and transcriptome analyses reveal genes involved in the formation of fine ridges on petal epidermal cells in Hibiscus trionum Chromosome-level genome assembly of Lilford’s wall lizard, Podarcis lilfordi (Günther, 1874) from the Balearic Islands (Spain) Mituru Takanami, 1929–2022 A highly contiguous genome assembly of red perilla (Perilla frutescens) domesticated in Japan
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1