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1.
Nature ; 387(6632 Suppl): 87-90, 1997 May 29.
Article in English | MEDLINE | ID: mdl-9169871

ABSTRACT

The yeast Saccharomyces cerevisiae is the pre-eminent organism for the study of basic functions of eukaryotic cells. All of the genes of this simple eukaryotic cell have recently been revealed by an international collaborative effort to determine the complete DNA sequence of its nuclear genome. Here we describe some of the features of chromosome XII.


Subject(s)
Chromosomes, Fungal , Saccharomyces cerevisiae/genetics , Base Sequence , DNA, Fungal , Molecular Sequence Data
2.
Nature ; 387(6632 Suppl): 93-8, 1997 May 29.
Article in English | MEDLINE | ID: mdl-9169873

ABSTRACT

In 1992 we started assembling an ordered library of cosmid clones from chromosome XIV of the yeast Saccharomyces cerevisiae. At that time, only 49 genes were known to be located on this chromosome and we estimated that 80% to 90% of its genes were yet to be discovered. In 1993, a team of 20 European laboratories began the systematic sequence analysis of chromosome XIV. The completed and intensively checked final sequence of 784,328 base pairs was released in April, 1996. Substantial parts had been published before or had previously been made available on request. The sequence contained 419 known or presumptive protein-coding genes, including two pseudogenes and three retrotransposons, 14 tRNA genes, and three small nuclear RNA genes. For 116 (30%) protein-coding sequences, one or more structural homologues were identified elsewhere in the yeast genome. Half of them belong to duplicated groups of 6-14 loosely linked genes, in most cases with conserved gene order and orientation (relaxed interchromosomal synteny). We have considered the possible evolutionary origins of this unexpected feature of yeast genome organization.


Subject(s)
Chromosomes, Fungal , Evolution, Molecular , Saccharomyces cerevisiae/genetics , Base Sequence , Molecular Sequence Data , Multigene Family , Open Reading Frames , Restriction Mapping
4.
J Virol ; 68(1): 379-89, 1994 Jan.
Article in English | MEDLINE | ID: mdl-8254750

ABSTRACT

A fresh inoculum of human adenovirus type 12 (Ad12) was obtained from the American Type Culture Collection and passaged once on human embryonic kidney cells, and Ad12 DNA was prepared from the first-passage yield to avoid higher passages which might have generated host-virus DNA recombinants. The 18 PstI fragments of Ad12 DNA were cloned into the pBluescript KS vector, and the entire nucleotide sequence of both strands from all 18 fragments was determined by using successive oligodeoxyribonucleotide primers. Ad12 DNA extends over 34,125 nucleotide pairs, and its molecular weight is calculated to be about 22 x 10(6). The nucleotide sequence of Ad12 DNA was subjected to computer analyses that determined possible open reading of frames on the two strands, the leader sequences, the position of the virus-associated RNA coding region, possible TATA, and polyadenylation signals. The distribution of the Ad12 open reading frames was similar to that in the previously sequenced Ad2 DNA, but there were also distinct differences. Ad12 DNA has an inverted terminal redundancy of 161 nucleotides, compared with 102 nucleotides in Ad2 DNA. There were stretches of sequence identity between Ad2 and Ad12 DNAs at both termini; the overall sequence similarity between the two viral genomes ranged between 59% (polypeptide IX) and 77% (in the E2 region), with high homology also in the sequences for the adenovirus DNA polymerase.


Subject(s)
Adenoviruses, Human/genetics , DNA, Viral/genetics , Genome, Viral , Base Composition , Base Sequence , DNA, Viral/chemistry , Molecular Sequence Data , Molecular Weight , Open Reading Frames , Promoter Regions, Genetic/genetics , Repetitive Sequences, Nucleic Acid/genetics , Restriction Mapping , Sequence Analysis, DNA , Sequence Homology, Nucleic Acid , Transcription, Genetic
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