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The DNA sequence, annotation and analysis of human chromosome 3
Authors:Muzny Donna M  Scherer Steven E  Kaul Rajinder  Wang Jing  Yu Jun  Sudbrak Ralf  Buhay Christian J  Chen Rui  Cree Andrew  Ding Yan  Dugan-Rocha Shannon  Gill Rachel  Gunaratne Preethi  Harris R Alan  Hawes Alicia C  Hernandez Judith  Hodgson Anne V  Hume Jennifer  Jackson Andrew  Khan Ziad Mohid  Kovar-Smith Christie  Lewis Lora R  Lozado Ryan J  Metzker Michael L  Milosavljevic Aleksandar  Miner George R  Morgan Margaret B  Nazareth Lynne V  Scott Graham  Sodergren Erica  Song Xing-Zhi  Steffen David  Wei Sharon  Wheeler David A  Wright Mathew W  Worley Kim C  Yuan Ye  Zhang Zhengdong  Adams Charles Q  Ansari-Lari M Ali
Affiliation:Human Genome Sequencing Center, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.
Abstract:
After the completion of a draft human genome sequence, the International Human Genome Sequencing Consortium has proceeded to finish and annotate each of the 24 chromosomes comprising the human genome. Here we describe the sequencing and analysis of human chromosome 3, one of the largest human chromosomes. Chromosome 3 comprises just four contigs, one of which currently represents the longest unbroken stretch of finished DNA sequence known so far. The chromosome is remarkable in having the lowest rate of segmental duplication in the genome. It also includes a chemokine receptor gene cluster as well as numerous loci involved in multiple human cancers such as the gene encoding FHIT, which contains the most common constitutive fragile site in the genome, FRA3B. Using genomic sequence from chimpanzee and rhesus macaque, we were able to characterize the breakpoints defining a large pericentric inversion that occurred some time after the split of Homininae from Ponginae, and propose an evolutionary history of the inversion.
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