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Nature ; 431(7006): 268-74, 2004 Sep 16.
Article in English | MEDLINE | ID: mdl-15372022

ABSTRACT

Chromosome 5 is one of the largest human chromosomes and contains numerous intrachromosomal duplications, yet it has one of the lowest gene densities. This is partially explained by numerous gene-poor regions that display a remarkable degree of noncoding conservation with non-mammalian vertebrates, suggesting that they are functionally constrained. In total, we compiled 177.7 million base pairs of highly accurate finished sequence containing 923 manually curated protein-coding genes including the protocadherin and interleukin gene families. We also completely sequenced versions of the large chromosome-5-specific internal duplications. These duplications are very recent evolutionary events and probably have a mechanistic role in human physiological variation, as deletions in these regions are the cause of debilitating disorders including spinal muscular atrophy.


Subject(s)
Chromosomes, Human, Pair 5/genetics , Sequence Analysis, DNA , Animals , Base Composition , Cadherins/genetics , Conserved Sequence/genetics , Gene Duplication , Genes/genetics , Genetic Diseases, Inborn/genetics , Genomics , Humans , Interleukins/genetics , Molecular Sequence Data , Muscular Atrophy, Spinal/genetics , Pan troglodytes/genetics , Physical Chromosome Mapping , Pseudogenes/genetics , Synteny/genetics , Vertebrates/genetics
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