Lyle Robert, Prandini Paola, Osoegawa Kazutoyo, ten Hallers Boudewijn, Humphray Sean, Zhu Baoli, Eyras Eduardo, Castelo Robert, Bird Christine P, Gagos Sarantos, Scott Carol, Cox Antony, Deutsch Samuel, Ucla Catherine, Cruts Marc, Dahoun Sophie, She Xinwei, Bena Frederique, Wang Sheng-Yue, Van Broeckhoven Christine, Eichler Evan E, Guigo Roderic, Rogers Jane, de Jong Pieter J, Reymond Alexandre, Antonarakis Stylianos E
Department of Genetic Medicine and Development, University of Geneva Medical School, and University Hospitals, 1211 Geneva, Switzerland.
Genome Res. 2007 Nov;17(11):1690-6. doi: 10.1101/gr.6675307. Epub 2007 Sep 25.
The goals of the human genome project did not include sequencing of the heterochromatic regions. We describe here an initial sequence of 1.1 Mb of the short arm of human chromosome 21 (HSA21p), estimated to be 10% of 21p. This region contains extensive euchromatic-like sequence and includes on average one transcript every 100 kb. These transcripts show multiple inter- and intrachromosomal copies, and extensive copy number and sequence variability. The sequencing of the "heterochromatic" regions of the human genome is likely to reveal many additional functional elements and provide important evolutionary information.
人类基因组计划的目标并不包括对异染色质区域进行测序。我们在此描述人类21号染色体短臂(HSA21p)1.1 Mb的初始序列,估计占21p的10%。该区域包含广泛的类常染色质序列,平均每100 kb有一个转录本。这些转录本显示出多个染色体间和染色体内的拷贝,以及广泛的拷贝数和序列变异性。对人类基因组“异染色质”区域的测序可能会揭示许多额外的功能元件,并提供重要的进化信息。