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1.
Nature ; 428(6982): 522-8, 2004 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-15057823

RESUMO

Chromosome 13 is the largest acrocentric human chromosome. It carries genes involved in cancer including the breast cancer type 2 (BRCA2) and retinoblastoma (RB1) genes, is frequently rearranged in B-cell chronic lymphocytic leukaemia, and contains the DAOA locus associated with bipolar disorder and schizophrenia. We describe completion and analysis of 95.5 megabases (Mb) of sequence from chromosome 13, which contains 633 genes and 296 pseudogenes. We estimate that more than 95.4% of the protein-coding genes of this chromosome have been identified, on the basis of comparison with other vertebrate genome sequences. Additionally, 105 putative non-coding RNA genes were found. Chromosome 13 has one of the lowest gene densities (6.5 genes per Mb) among human chromosomes, and contains a central region of 38 Mb where the gene density drops to only 3.1 genes per Mb.


Assuntos
Cromossomos Humanos Par 13/genética , Genes/genética , Mapeamento Físico do Cromossomo , Mapeamento Cromossômico , Genética Médica , Humanos , Pseudogenes/genética , RNA não Traduzido/genética , Análise de Sequência de DNA
2.
Nature ; 414(6866): 865-71, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11780052

RESUMO

The finished sequence of human chromosome 20 comprises 59,187,298 base pairs (bp) and represents 99.4% of the euchromatic DNA. A single contig of 26 megabases (Mb) spans the entire short arm, and five contigs separated by gaps totalling 320 kb span the long arm of this metacentric chromosome. An additional 234,339 bp of sequence has been determined within the pericentromeric region of the long arm. We annotated 727 genes and 168 pseudogenes in the sequence. About 64% of these genes have a 5' and a 3' untranslated region and a complete open reading frame. Comparative analysis of the sequence of chromosome 20 to whole-genome shotgun-sequence data of two other vertebrates, the mouse Mus musculus and the puffer fish Tetraodon nigroviridis, provides an independent measure of the efficiency of gene annotation, and indicates that this analysis may account for more than 95% of all coding exons and almost all genes.


Assuntos
Cromossomos Humanos Par 20 , Animais , Sequência de Bases , Biologia Computacional , Mapeamento de Sequências Contíguas , DNA , Doenças Genéticas Inatas/genética , Variação Genética , Humanos , Camundongos , Mapeamento Físico do Cromossomo , Proteoma , Análise de Sequência de DNA
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