RESUMEN
The Afrotropical mosquito Anopheles gambiae sensu stricto, a major vector of malaria, is currently undergoing speciation into the M and S molecular forms. These forms have diverged in larval ecology and reproductive behavior through unknown genetic mechanisms, despite considerable levels of hybridization. Previous genome-wide scans using gene-based microarrays uncovered divergence between M and S that was largely confined to gene-poor pericentromeric regions, prompting a speciation-with-ongoing-gene-flow model that implicated only about 3% of the genome near centromeres in the speciation process. Here, based on the complete M and S genome sequences, we report widespread and heterogeneous genomic divergence inconsistent with appreciable levels of interform gene flow, suggesting a more advanced speciation process and greater challenges to identify genes critical to initiating that process.
Asunto(s)
Anopheles/genética , Especiación Genética , Genoma de los Insectos , Animales , Anopheles/clasificación , Evolución Molecular , Femenino , Flujo Génico , Masculino , Modelos Genéticos , Polimorfismo de Nucleótido SimpleRESUMEN
With an aim to clone the sorghum fertility restorer gene Rf1, a high-resolution genetic and physical map of the locus was constructed. The Rf1 locus was resolved to a 32-kb region spanning four open reading frames: a plasma membrane Ca(2+)-ATPase, a cyclin D-1, an unknown protein, and a pentatricopeptide repeat (PPR13) gene family member. An approximately 19-kb region spanning the cyclin D-1 and unknown protein genes was completely conserved between sterile and fertile plants as was the sequence spanning the coding region of the Ca(2+)-ATPase. In contrast, 19 sequence polymorphisms were located in an approximately 7-kb region spanning PPR13, and all markers cosegregated with the fertility restoration phenotype. PPR13 was predicted to encode a mitochondrial-targeted protein containing a single exon with 14 PPR repeats, and the protein is classified as an E-type PPR subfamily member. To permit sequence-based comparison of the sorghum and rice genomes in the Rf1 region, 0.53 Mb of sorghum chromosome 8 was sequenced and compared to the colinear region of rice chromosome 12. Genome comparison revealed a mosaic pattern of colinearity with an approximately 275-kb gene-poor region with little gene conservation and an adjacent, approximately 245-kb gene-rice region that is more highly conserved between rice and sorghum. Despite being located in a region of high gene conservation, sorghum PPR13 was not located in a colinear position on rice chromosome 12. The present results suggest that sorghum PPR13 represents a potential candidate for the sorghum Rf1 gene, and its presence in the sorghum genome indicates a single gene transposition event subsequent to the divergence of rice and sorghum ancestors.
Asunto(s)
Evolución Molecular , Genes de Plantas/genética , Oryza/genética , Fenotipo , Mapeo Físico de Cromosoma , Polimorfismo Genético , Sorghum/genética , Secuencia de Aminoácidos , Secuencia de Bases , Cromosomas Artificiales Bacterianos , Cartilla de ADN , Fertilidad/genética , Componentes del Gen , Datos de Secuencia Molecular , Secuencias Repetitivas de Ácidos Nucleicos/genética , Análisis de Secuencia de ADNAsunto(s)
Análisis Mutacional de ADN/métodos , Genoma Humano , Mutación , Cartilla de ADN , Humanos , Recién Nacido , Leucemia Mieloide Aguda/genética , Masculino , Reacción en Cadena de la Polimerasa/métodos , Neoplasias de la Próstata/genética , Proteína B Asociada a Surfactante Pulmonar/deficiencia , Proteína B Asociada a Surfactante Pulmonar/genética , Síndrome de Dificultad Respiratoria del Recién Nacido/genéticaRESUMEN
Deletions of the AZFc (azoospermia factor c) region of the Y chromosome are the most common known cause of spermatogenic failure. We determined the complete nucleotide sequence of AZFc by identifying and distinguishing between near-identical amplicons (massive repeat units) using an iterative mapping-sequencing process. A complex of three palindromes, the largest spanning 3 Mb with 99.97% identity between its arms, encompasses the AZFc region. The palindromes are constructed from six distinct families of amplicons, with unit lengths of 115-678 kb, and may have resulted from tandem duplication and inversion during primate evolution. The palindromic complex contains 11 families of transcription units, all expressed in testis. Deletions of AZFc that cause infertility are remarkably uniform, spanning a 3.5-Mb segment and bounded by 229-kb direct repeats that probably served as substrates for homologous recombination.
Asunto(s)
Deleción Cromosómica , Infertilidad Masculina/genética , Cromosoma Y/genética , Secuencia de Bases , Inversión Cromosómica , Cromosomas Humanos Par 3/genética , Proteína 1 Delecionada en la Azoospermia , Evolución Molecular , Duplicación de Gen , Humanos , Masculino , Modelos Genéticos , Datos de Secuencia Molecular , Oligospermia/genética , Especificidad de Órganos , Mapeo Físico de Cromosoma , Proteínas de Unión al ARN/genética , Recombinación Genética/genética , Análisis de Secuencia de ADN , Eliminación de Secuencia/genética , Homología de Secuencia de Ácido Nucleico , Espermatozoides/metabolismo , Secuencias Repetidas en Tándem/genética , Testículo/metabolismo , Transcripción Genética/genéticaRESUMEN
The identification of the cystic fibrosis transmembrane conductance regulator gene (CFTR) in 1989 represents a landmark accomplishment in human genetics. Since that time, there have been numerous advances in elucidating the function of the encoded protein and the physiological basis of cystic fibrosis. However, numerous areas of cystic fibrosis biology require additional investigation, some of which would be facilitated by information about the long-range sequence context of the CFTR gene. For example, the latter might provide clues about the sequence elements responsible for the temporal and spatial regulation of CFTR expression. We thus sought to establish the sequence of the chromosomal segments encompassing the human CFTR and mouse Cftr genes, with the hope of identifying conserved regions of biologic interest by sequence comparison. Bacterial clone-based physical maps of the relevant human and mouse genomic regions were constructed, and minimally overlapping sets of clones were selected and sequenced, eventually yielding approximately 1.6 Mb and approximately 358 kb of contiguous human and mouse sequence, respectively. These efforts have produced the complete sequence of the approximately 189-kb and approximately 152-kb segments containing the human CFTR and mouse Cftr genes, respectively, as well as significant amounts of flanking DNA. Analyses of the resulting data provide insights about the organization of the CFTR/Cftr genes and potential sequence elements regulating their expression. Furthermore, the generated sequence reveals the precise architecture of genes residing near CFTR/Cftr, including one known gene (WNT2/Wnt2) and two previously unknown genes that immediately flank CFTR/Cftr.