1. DNA sequence and analysis of human chromosome 9.
- Author
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Humphray, S.J., Oliver, K., Hunt, A.R., Plumb, R.W., Loveland, J.E., Howe, K.L., Andrews, T.D., Searle, S., Hunt, S.E., Scott, C.E., Jones, M.C., Ainscough, R., Almeida, J.P., Ambrose, K.D., Ashwell, R.I.S., Babbage, A.K., Babbage, S., Bagguley, C.L., Bailey, J., and Banerjee, R.
- Subjects
HUMAN chromosomes ,HUMAN genetics ,NUCLEOTIDE sequence ,HETEROCHROMATIN ,INTERFERONS ,HUMAN genome - Abstract
Chromosome 9 is highly structurally polymorphic. It contains the largest autosomal block of heterochromatin, which is heteromorphic in 6-8% of humans, whereas pericentric inversions occur in more than 1% of the population. The finished euchromatic sequence of chromosome 9 comprises 109,044,351 base pairs and represents >99.6% of the region. Analysis of the sequence reveals many intra- and interchromosomal duplications, including segmental duplications adjacent to both the centromere and the large heterochromatic block. We have annotated 1,149 genes, including genes implicated in male-to-female sex reversal, cancer and neurodegenerative disease, and 426 pseudogenes. The chromosome contains the largest interferon gene cluster in the human genome. There is also a region of exceptionally high gene and G + C content including genes paralogous to those in the major histocompatibility complex. We have also detected recently duplicated genes that exhibit different rates of sequence divergence, presumably reflecting natural selection. [ABSTRACT FROM AUTHOR]
- Published
- 2004
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