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1.
The rat genome project and the resources that it has generated are transforming the translation of rat biology to human medicine. The rat genome was sequenced to a high quality "draft," the structure and location of the genes were predicted, and a global assessment was published (Gibbs RA et al., Nature 428: 493-521, 2004). Since that time, researchers have made use of the genome sequence and annotations and related resources. We take this opportunity to review the currently available rat genome resources and to discuss the progress and future plans for the rat genome. 相似文献
2.
High-throughput scanning of the rat genome using interspersed repetitive sequence-PCR markers 总被引:4,自引:0,他引:4
Gösele C Hong L Kreitler T Rossmann M Hieke B Gross U Kramer M Himmelbauer H Bihoreau MT Kwitek-Black AE Twigger S Tonellato PJ Jacob HJ Schalkwyk LC Lindpaintner K Ganten D Lehrach H Knoblauch M 《Genomics》2000,69(3):287-294
We report the establishment of a hybridization-based marker system for the rat genome based on the PCR amplification of interspersed repetitive sequences (IRS). Overall, 351 IRS markers were mapped within the rat genome. The IRS marker panel consists of 210 nonpolymorphic and 141 polymorphic markers that were screened for presence/absence polymorphism patterns in 38 different rat strains and substrains that are commonly used in biomedical research. The IRS marker panel was demonstrated to be useful for rapid genome screening in experimental rat crosses and high-throughput characterization of large-insert genomic library clones. Information on corresponding YAC clones is made available for this IRS marker set distributed over the whole rat genome. The two existing rat radiation hybrid maps were integrated by placing the IRS markers in both maps. The genetic and physical mapping data presented provide substantial information for ongoing positional cloning projects in the rat. 相似文献
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The DNA-binding nonhistone proteins (NHP) have been demonstrated to fractionate the rat genome into protein-bound and unbound DNA sequences. Twenty percent of highly sheared rat DNA [approximately 350 base pair (bp)] can be retained on membrane filters as protein complexes. When extracted from the filter and retitrated with the NHP, a 4- to 5-fold enrichment of binding sites is present in the bound DNA with few, if any, sites detected in the unbound DNA. Rat DNA restricted by EcoRI endonuclease can be fractionated by its DNA-binding NHP retention characteristics. Reassociation kinetics of the bound restricted sequences indicate that 45.6% is a subset of total single-copy sequence of the rat genome an 26.9% is repetitive sequences. Cross hybridization studies indicate the repetitive sequences of the bound DNA are not enriched as much as the slow component of the rat genome. Thus a 4-fold enrichment of a subset of the rat genome has been observed via NHP-DNA interactions. 相似文献
5.
Khulood M. Al-Majali Anne M. Glazier Penny J. Norsworthy Faisal N. Wahid Lisa D. Cooper Caroline A. Wallace James Scott Berthold Lausen Timothy J. Aitman 《Mammalian genome》1999,10(5):471-476
Radiation hybrid (RH) mapping has been used to produce genome maps in the human and mouse, but as yet the technique has been
applied little to other species. We describe the use of RH mapping in the rat, using a newly available rat/hamster RH panel,
to construct an RH map of the proximal part of rat Chromosome (Chr) 4. This region is of interest because quantitative trait
loci (QTLs) for defective insulin and catecholamine action, hypertension, and dyslipidemia map to this region. The RH map
includes 23 rat genes or microsatellites previously mapped to this part of Chr 4, one rat gene not previously mapped in the
rat, and markers for four new genes, homologs of which map to the syntenic region of the mouse genome. The RH map integrates
genetic markers previously mapped on several rat crosses, increases the resolution of existing maps, and may provide a suitable
basis for physical map construction and gene identification in this chromosomal region. Our results demonstrate the utility
of RH mapping in the rat genome and show that RH mapping can be used to localize, in the rat genome, the homologs of genes
from other species such as the mouse. This will facilitate identification of candidate genes underlying QTLs on this chromosomal
segment.
Received: 4 December 1998 / Accepted: 19 January 1999 相似文献
6.
More than a thousand quantitative trait loci (QTLs) relevant to many aspects of complex human disease have been identified in a wide range of rat inbred lines over the past few decades. With the complete rat genome available, it is now time for the next stage in rat genetic research: the identification and causal confirmation of underlying polymorphisms and genes. Recent developments in single nucleotide polymorphism-based genetic markers and technologies to manipulate the rat genome will undoubtedly be important tools in this next episode. 相似文献
7.
gamma-Glutamyl transpeptidase: a single copy gene in the rat and a multigene family in the human genome 总被引:5,自引:0,他引:5
A Pawlak O Lahuna F Bulle A Suzuki N Ferry S Siegrist N Chikhi M N Chobert G Guellaen Y Laperche 《The Journal of biological chemistry》1988,263(20):9913-9916
gamma-Glutamyl transpeptidase (GGT) genomic sequences were isolated from rat and human libraries using a rat GGT cDNA as a cross-species hybridization probe. Characterization of the human GGT clones by restriction mapping clearly establishes that at least four different GGT genes or pseudogenes are present in the human genome. All the rat genomic clones cover a 12.5-kilobase sequence and exhibit a unique restriction pattern. A precise quantitation of the rat GGT gene copy number by Southern blot analysis demonstrates that this sequence is present as a single copy/rat haploid genome. Therefore, the GGT gene organization is different between rat and human species; this raises the possibility of different regulatory mechanisms in the two species. 相似文献
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Dominique Gauguier Pamela J. Kaisaki Mathias Rouard Robert H. Wallis Julie Browne John P. Rapp Marie-Thérèse Bihoreau 《Mammalian genome》1999,10(7):675-686
We report the localization by linkage analysis in the rat genome of 148 new markers derived from 128 distinct known gene
sequences, ESTs, and anonymous sequences selected in GenBank database on the basis of the presence of a repeated element.
The composite linkage map of the rat contributed by our group integrates mapping information on a total of 370 different known
genes, ESTs, and anonymous mouse or human sequences, and provides a valuable tool for comparative genome analysis. 206 and
254 homologous loci were identified in the mouse and human genomes respectively. Our linkage map, which combines both anonymous
markers and gene markers, should facilitate the advancement of genetic studies for a wide variety of rat models characterized
for complete phenotypes. The comparative genome mapping should define genetic regions in human likely to be homologous to
susceptibility loci identified in rat and provide useful information for the identification of new potential candidates for
genetic disorders.
Received: 2 January 1999 / Accepted: 7 March 1999 相似文献
10.
Adenovirus type 12-transformed rat embryo brain and rat liver epithelial cell lines: adenovirus type 12 genome content and viral protein expression. 总被引:3,自引:1,他引:2
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By Southern blotting analysis, six adenovirus type 12 (Ad-12)-transformed rat embryo brain cell lines and one Ad-12-transformed rat liver epithelial line were shown to contain all or nearly all the Ad-12 genome. Another Ad-12 rat liver epithelial cell line contained a repeating structure consisting of only the left-hand 16% of the Ad-12 genome. Three Ad-12-specified proteins (molecular weights, 52,000, 41,000, and 18,000) were found by immunoprecipitation to be common to all of these cell lines. Two rat liver epithelial lines, produced from an Ad-12-infected culture and previously shown to be T-antigen negative by immunofluorescence, contained no detectable Ad-12 genome or Ad-12-specified proteins. Although some of the rat embryo brain transformants had been shown previously to express "late" Ad-12 mRNA, no Ad-12 structural proteins were found to be produced by these cell lines. 相似文献
11.
Sugino H 《FEBS letters》2007,581(3):355-360
The rat and mouse amylase gene families were characterized using sequence data from the UCSC genome assembly. We found that the rat genome contains one amylase-1 and two amylase-2 genes, lying close to one another on the same chromosome. Detailed analysis revealed at least six additional amylase pseudogenes in the rat genome in the region adjacent to the amylase-2 genes. In contrast, the mouse has one amylase-1 gene and five amylase-2 genes; the latter are tandemly and systematically arranged on the same chromosome and were generated by segmental duplication. Detailed analysis revealed that the mouse has two amylase pseudogenes, located 5' to the five amylase-2 segments. Thus, the amylase genes of mouse and rat tend to be amplified; the sequences of some of them are fixed while others have become pseudogenes during evolution. This is the second report of amylase genomic organization in mammals and the first in the rodents. 相似文献
12.
Finding the position of a gene is now easily done when the genome sequence is available: the gene position is generally found by a simple query of genomic databases such as those available at the Ensembl browser or the NCBI. We were interested in determining the position of 125 cancer-related rat genes and we found that the position of most of these genes (110) could indeed be identified in this manner. However, in 15 cases, the gene position was not available in these databases, or the results were ambiguous. We then explored a more specialized database, namely the Rat Genome Database, and experimentally mapped these genes using standard and radiation cell hybrids. The 15 genes in question could be localized unambiguously. In four cases, the radiation cell hybrids were indispensable: the sequence of these four genes could not be found in the rat genome sequence. On the basis of the sample we examined, it thus appears that a classical gene mapping method is still required to localize about 3% of the rat genes, as if 3% of the rat gene sequences were lacking in the current rat genome sequence. 相似文献
13.
FBJ osteosarcoma virus in tissue culture. III. Isolation and characterization of non-virus-producing FBJ-transformed cells. 总被引:4,自引:1,他引:3
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Hamster and rat cell lines have been established that have been transformed by FBJ murine sarcoma virus (FBJ-MuSV) but that do not produce virus. The hamster cell line originated from an osteosarcoma that appeared in a hamster inoculated at birth with an extract of a CFNo1 mouse FBJ-osteosarcoma. The rat cell line was obtained by transferring the FBJ-MuSV genome to normal rat kidney cells in the absence of the FBJ type C virus (FBJ-MuLV), which, usually in high concentration, accompanies the FBJ-MuSV. Both transformed hamster and rat cell lines contain the FBJ-MuSV genome, which can be rescued by ecotropic and xenotropic murine type C viruses. This rescued genome produces characteristic FBJ-MuSV foci in tissue culture and, in appropriate animal hosts, induces osteosarcomas typical of those induced by FBJ-MuSV. FBJ-MuSV was isolated originally from a parosteal osteosarcoma that occurred naturally in a mouse. Since there was no previous history of passage of the agent through any other animal species, these non-virus-producing hamster and rat cells transformed by FBJ-MuSV should be very helpful in molecular studies examining the origin of spontaneous sarcoma genomes in mice. 相似文献
14.
Iddm4 is one of several susceptibility genes that have been identified in the BB rat model of type 1 diabetes. The BB rat allele of this gene confers dominant predisposition to diabetes induction by immune perturbation in both the diabetes-prone and the diabetes-resistant substrains, whereas the Wistar Furth (WF) allele confers resistance. We have positioned the gene in a 2.8-cM region on rat Chromosome (Chr) 4, proximal to Lyp/Ian4l1. We have produced a radiation hybrid map of the Iddm4-region that includes a number of rat genes with their mouse and human orthologs. We present a comparative map of the rat Iddm4 region in rat, human, and mouse, assigning the gene to a 6.3-Mb segment between PTN and ZYX at 7q32 in the human genome, and to a 5.7-Mb segment between Ptn and Zyx in the mouse genome. 相似文献
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Examination of the Rattus norvegicus genome reveals differences in the melanocortin 3 receptor (MC3R) compared with the published sequence (accession X70667). To clarify these differences, we used RT-PCR to clone MC3R from Sprague Dawley rats. These efforts revealed a sequence for the rat MC3R consistent with that predicted by the rat genome, but different from the published receptor by three amino acids, all of which were located in the predicted second transmembrane domain (TM2). Analysis of these residues revealed that TM2 of the rat MC3R is more homologous with other species than previously considered. The presently described sequence maps onto chromosome 3 of the rat genome, which shows highly conserved synteny with the mouse chromosome 2 and the human chromosome 20. Transient expression revealed high affinity binding of [125I]-NDP-MSH and a concentration-dependent cAMP response to the synthetic agonist MTII. These data both clarify the sequence of the MC3R and demonstrate the great utility of genomic information recently made available. 相似文献
17.
Peng Yeong Woon Kazutoyo Osoegawa Pamela J. Kaisaki Baohui Zhao Joseph J. Catanese Dominique Gauguier Roger Cox Elaine R. Levy G.Mark Lathrop Anthony P. Monaco Pieter J. de Jong 《Genomics》1998,50(3):306
A rat PAC library was constructed in the vector pPAC4 from genomic DNA isolated from female Brown Norway rats. This library consists of 215,409 clones arrayed in 614 384-well microtiter plates. An average insert size of 143 kb was estimated from 217 randomly isolated clones, thus representing approximately 10-fold genome coverage. This coverage provides a very high probability that the library contains a unique sequence in genome screening. Tests on randomly selected clones demonstrated that they are very stable, with only 4 of 130 clones showing restriction digest fragment alterations after 80 generations of serial growth. FISH analysis using 70 randomly chosen PACs revealed no significant chimeric clones. About 7% of the clones analyzed contained repetitive sequences related to centromeric regions that hybridized to some but not all centromeres. DNA plate pools and superpools were made, and high-density filters each containing an array of 8 plates in duplicate were prepared. Library screening on these superpools and appropriate filters with 10 single-locus rat markers revealed an average of 8 positive clones, in agreement with the estimated high genomic coverage of this library and representation of the rat genome. This library provides a new resource for rat genome analysis, in particular the identification of genes involved in models of multifactorial disease. The library and high-density filters are currently available to the scientific community. 相似文献
18.
A recombinant plasmid containing four tandem head-to-tail copies of the HBV4 genome has been constructed and introduced into thymidine kinase-deficient mouse and rat fibroblast cells by co-transformation with the thymidine kinase gene from Herpes simplex virus as a selectable marker. Several mouse cell lines that synthesize HBsAg and four lines (three mouse and one rat) that synthesize both HBsAg and HBeAg were isolated. The rat line and at least one of the L cell lines that synthesizes HBeAg also produce small quantities of HBcAg. The rat line has many partial and 18 to 20 complete copies of the HBV genome integrated into high molecular weight DNA, whereas the L cells that produce HBeAg have only two to three complete copies of HBV genome. The kinetics of synthesis of HBsAg and HBeAg by the rat line are similar to that for HBsAg synthesis by two human hepatoma lines, and the HBsAg secreted by this line has similar biophysical characteristics to that found in human serum. The results suggest that the configuration of the recombinant molecule used may be an important prerequisite for the expression of HBcAg and HBeAg, and we speculate that the biogenesis of their messenger RNA may proceed via a precursor that is greater than the length of the HBV genome. 相似文献
19.
Xiaosen Guo Max Brenner Xuemei Zhang Teresina Laragione Shuaishuai Tai Yanhong Li Junjie Bu Ye Yin Anish A. Shah Kevin Kwan Yingrui Li Wang Jun Pércio S. Gulko 《Genetics》2013,194(4):1017-1028
DA (D-blood group of Palm and Agouti, also known as Dark Agouti) and F344 (Fischer) are two inbred rat strains with differences in several phenotypes, including susceptibility to autoimmune disease models and inflammatory responses. While these strains have been extensively studied, little information is available about the DA and F344 genomes, as only the Brown Norway (BN) and spontaneously hypertensive rat strains have been sequenced to date. Here we report the sequencing of the DA and F344 genomes using next-generation Illumina paired-end read technology and the first de novo assembly of a rat genome. DA and F344 were sequenced with an average depth of 32-fold, covered 98.9% of the BN reference genome, and included 97.97% of known rat ESTs. New sequences could be assigned to 59 million positions with previously unknown data in the BN reference genome. Differences between DA, F344, and BN included 19 million positions in novel scaffolds, 4.09 million single nucleotide polymorphisms (SNPs) (including 1.37 million new SNPs), 458,224 short insertions and deletions, and 58,174 structural variants. Genetic differences between DA, F344, and BN, including high-impact SNPs and short insertions and deletions affecting >2500 genes, are likely to account for most of the phenotypic variation between these strains. The new DA and F344 genome sequencing data should facilitate gene discovery efforts in rat models of human disease. 相似文献
20.
Highly repeated DNA families in the rat 总被引:19,自引:0,他引:19
We have analyzed the repeated DNA fraction of the rat by characterizing approximately 500 repeat DNA-containing clones using hybridization to a variety of rodent nucleic acids. To facilitate this analysis we devised a method whereby the cloned DNA is transferred to nitrocellulose paper by blotting directly out of colonies of the bacterial clones. In addition to identifying repeated sequences of potential interest (e.g. those transcribed in a tissue-specific manner, or those that are highly conserved in non-rat genomes), we found that, in contrast to what is revealed by the reassociation of rat DNA (e.g. Pearson, W. R., Wu, J. R., and Bonner, J. (1978) Biochemistry 17, 51-59), the rat genome contains a number of different highly repeated (greater than 50,000 copies) sequences. We distinguished the different highly repeated sequences both by their hybridization to different nucleic acids as well as by DNA sequence determination. The highly repeated sequences shared three characteristics that distinguished each of them from the 100,000-member rat satellite I family: (i) they were recovered less often in the cloned repeat DNA library than expected from their copy number in the rat genome; (ii) they reannealed abnormally slowly for their copy number even though they are not significantly divergent; and (iii) they are transcribed in one or more rat tissues. The implications of these findings for the organization of repeated sequences in the rat genome are discussed. 相似文献