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1.
PLoS Genet ; 5(11): e1000728, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19936048

RESUMO

Most of our understanding of plant genome structure and evolution has come from the careful annotation of small (e.g., 100 kb) sequenced genomic regions or from automated annotation of complete genome sequences. Here, we sequenced and carefully annotated a contiguous 22 Mb region of maize chromosome 4 using an improved pseudomolecule for annotation. The sequence segment was comprehensively ordered, oriented, and confirmed using the maize optical map. Nearly 84% of the sequence is composed of transposable elements (TEs) that are mostly nested within each other, of which most families are low-copy. We identified 544 gene models using multiple levels of evidence, as well as five miRNA genes. Gene fragments, many captured by TEs, are prevalent within this region. Elimination of gene redundancy from a tetraploid maize ancestor that originated a few million years ago is responsible in this region for most disruptions of synteny with sorghum and rice. Consistent with other sub-genomic analyses in maize, small RNA mapping showed that many small RNAs match TEs and that most TEs match small RNAs. These results, performed on approximately 1% of the maize genome, demonstrate the feasibility of refining the B73 RefGen_v1 genome assembly by incorporating optical map, high-resolution genetic map, and comparative genomic data sets. Such improvements, along with those of gene and repeat annotation, will serve to promote future functional genomic and phylogenomic research in maize and other grasses.


Assuntos
Pareamento de Bases/genética , Genoma de Planta/genética , Zea mays/genética , Sequência de Bases , Cromossomos de Plantas/genética , Elementos de DNA Transponíveis/genética , Evolução Molecular , Duplicação Gênica , Rearranjo Gênico/genética , Genes de Plantas , Loci Gênicos/genética , Dados de Sequência Molecular , Mutação/genética , Fases de Leitura Aberta/genética , Oryza/genética , Mapeamento Físico do Cromossomo , RNA de Plantas/genética , Homologia de Sequência do Ácido Nucleico , Sorghum/genética , Sintenia/genética
2.
Cancer Cell ; 3(3): 297-302, 2003 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-12676587

RESUMO

Representational difference analysis (RDA) of human breast cancer was used to discover a novel amplicon located at chromosomal region 8q24.3. We examined a series of breast cancer samples harboring amplification of this region and determined that KCNK9 is the sole overexpressed gene within the amplification epicenter. KCNK9 encodes a potassium channel that is amplified from 3-fold to 10-fold in 10% of breast tumors and overexpressed from 5-fold to over 100-fold in 44% of breast tumors. Overexpression of KCNK9 in cell lines promotes tumor formation and confers resistance to both hypoxia and serum deprivation, suggesting that its amplification and overexpression plays a physiologically important role in human breast cancer.


Assuntos
Amplificação de Genes , Canais de Potássio/genética , Canais de Potássio/metabolismo , Animais , Neoplasias da Mama/genética , Linhagem Celular , Transplante de Células , Cromossomos Humanos Par 8 , Sondas de DNA , Feminino , Regulação Neoplásica da Expressão Gênica , Genoma Humano , Humanos , Camundongos , Dados de Sequência Molecular , Oncogenes , Mapeamento Físico do Cromossomo , Sitios de Sequências Rotuladas , Transplante Heterólogo
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