Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 26
Filter
Add more filters










Publication year range
1.
Genome Res ; 14(7): 1438-43, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15231757

ABSTRACT

Single nucleotide polymorphisms (SNPs) are the most common source of genetic variation in populations and are thus most likely to account for the majority of phenotypic and behavioral differences between individuals or strains. Although the rat is extensively studied for the latter, data on naturally occurring polymorphisms are mostly lacking. We have used publicly available sequences consisting of whole-genome shotgun (WGS), expressed sequence tag (EST), and mRNA data as a source for the in silico identification of SNPs in gene-coding regions and have identified a large collection of 33,305 high-quality candidate SNPs. Experimental verification of 471 candidate SNPs using a limited set of rat isolates revealed a confirmation rate of approximately 50%. Although the majority of SNPs were identified between Sprague-Dawley (EST data) and Brown Norway (WGS data) strains, we found that 66% of the verified variations are common among different rat strains. All SNPs were extensively annotated, including chromosomal and genetic map information, and nonsynonymous SNPs were analyzed by SIFT and PolyPhen prediction programs for their potential deleterious effect on protein function. Interestingly, we retrieved three SNPs from the database that result in the introduction of a premature stop codon and that could be confirmed experimentally. Two of these "in silico-identified knockouts" reside in interesting QTL regions. Data are publicly available via a Web interface (http://cascad.niob.knaw.nl), allowing simple and advanced search queries.


Subject(s)
Expressed Sequence Tags , Polymorphism, Single Nucleotide/genetics , Animals , Databases, Genetic , Phylogeny , Polymorphism, Single Nucleotide/physiology , Predictive Value of Tests , Proteins/physiology , Rats , Rats, Inbred BN/genetics , Rats, Inbred BUF/genetics , Rats, Inbred F344/genetics , Rats, Inbred Lew/genetics , Rats, Inbred SHR/genetics , Rats, Sprague-Dawley/genetics , Software , Software Validation
3.
Muscle Nerve ; 21(12): 1655-60, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9843065

ABSTRACT

The mechanism of muscle weakness in myasthenia gravis and its possible relation to antibodies that are directed against the ryanodine receptor (RyR) were studied by the use of the spontaneous thymoma rat (Buffalo/Mna strain). The present study focused on the motor dysfunction as complicated by impaired subcellular machineries and noted particularly in patients with thymus abnormalities. Rats began to develop skeletal muscle weakness soon after birth and worsened progressively. Rats aged 3 months showed a benign thymoma characterized by proliferative lymphocytes; epithelial cells were stained with anti-RyR peptide antibody. The rat serum contained anti-RyR antibodies, but no anti-acetylcholine receptor antibodies. The electrophysiological study in muscle showed a reduction of contractile force without abnormality in synaptic transmission and membrane properties, suggesting a defect in excitation-contraction coupling. Hypothetically, thymic epithelial cells and skeletal muscles share a common RyR antigen, so that anti-RyR antibodies that target the thymic tissue may react with a homologous target in the muscle.


Subject(s)
Antibodies/immunology , Muscle Weakness/immunology , Myasthenia Gravis/immunology , Ryanodine Receptor Calcium Release Channel/immunology , Animals , Electrophysiology , Isometric Contraction/physiology , Muscle Weakness/physiopathology , Myasthenia Gravis/genetics , Myasthenia Gravis/pathology , Myasthenia Gravis/physiopathology , Rats , Rats, Inbred BUF/genetics , Rats, Inbred BUF/physiology , Thymoma/genetics , Thymus Gland/pathology , Thymus Neoplasms/genetics
4.
Muscle Nerve ; 20(10): 1258-63, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9324082

ABSTRACT

BUF/Mna strain rats spontaneously develop slowly progressing mild-moderate muscle atrophy of extensor digitorum longus, tibialis, and extraocular muscles, which consist mainly of fast-twitch type fibers, at nearly 100% incidence. They have lighter extensor digitorum longus muscles than soleus muscles, when alive for more than 6 weeks. Genetic segregation of the development of the muscle atrophy was studied by crossing the BUF/ Mna strain with three other strains, ACI/NMs, WKY/NCrj, and BDIX, which were free of muscle atrophy. Two autosomal dominant susceptible genes, Mas-1 and Mas-2, determine the development of the muscle atrophy in these combinations of crosses.


Subject(s)
Gene Expression Regulation , Muscle Fibers, Fast-Twitch/physiology , Muscular Atrophy/genetics , Muscular Atrophy/physiopathology , Rats, Inbred BUF/genetics , Rats, Inbred BUF/physiology , Animals , Disease Progression , Genes, Dominant , Genetic Predisposition to Disease , Hybridization, Genetic , Rats , Rats, Inbred Strains/genetics
5.
Mamm Genome ; 7(7): 505-8, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8672128

ABSTRACT

The thymoma-prone BUF/Mna rat is a useful model for human thymoma. Thymoma develops spontaneously in these rats at an incidence of nearly 100%. At pre-thymoma age, BUF/Mna rats have extremely large thymuses when compared with those of rats of the other strains, suggesting the presence of genes that regulate the thymus enlargement. We performed linkage study to identify the genetic loci associated with thymus enlargement in {(WKY/NCrj x BUF/Mna) F1 x BUF/Mna} backcross rats. Linkage study showed the significant associations between thymus size and markers on Chromosomes (Chrs) 1 and 13, suggesting the presence of two genes, Ten-1 and Ten-2, which regulate the thymus enlargement. Ten-1 was located between myosin light chain, muscle 2 (MYL2) and D1Mgh11 loci on Chr 1, and Ten-2 was located between synaptotagmin II (SYT2) and D13N2 loci on Chr 13.


Subject(s)
Chromosome Mapping , Rats, Inbred BUF/genetics , Thymoma/genetics , Thymus Gland/pathology , Thymus Neoplasms/genetics , Animals , Carrier Proteins/genetics , Crosses, Genetic , Female , Genetic Linkage , Genetic Markers , Humans , Lod Score , Male , Myosin Light Chains/genetics , Nerve Tissue Proteins/genetics , Rats , Rats, Inbred WKY , Recombination, Genetic , Synaptotagmin II , Thymus Gland/anatomy & histology
6.
Jpn J Cancer Res ; 87(7): 669-75, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8698613

ABSTRACT

The number of genetic markers for the rat is still limited, in spite of its wide use in cancer research. To facilitate accurate mapping of both established and novel rat genetic markers, we constructed a linkage map by genotyping 105 F2 rats from ACI/N (ACI) and BUF/Nac (BUF) crosses. This map consists of 120 genetic markers that had been previously reported, mainly by two research groups, but had not been integrated. To find new genetic markers, the arbitrarily primed polymerase chain reaction (AP-PCR) was applied to detect polymorphic bands between ACI and BUF rats. After testing 56 single primers and 12 combinations of primers, we found 36 bands produced by 16 single primers and two combinations to be reliably polymorphic between ACI and BUF rats. The 36 bands were typed in the 105 F2 rats, and 29 of them could be linkage-mapped. AP-PCR is thus useful to detect new genetic markers in laboratory strains of rats.


Subject(s)
Genetic Markers , Polymerase Chain Reaction , Rats, Inbred ACI/genetics , Rats, Inbred BUF/genetics , Animals , Base Sequence , Female , Genetic Linkage , Male , Molecular Sequence Data , Rats
7.
Proc Natl Acad Sci U S A ; 93(9): 3914-9, 1996 Apr 30.
Article in English | MEDLINE | ID: mdl-8632989

ABSTRACT

Representational difference analysis (RDA) was applied to isolate chromosomal markers in the rat. Four series of RDA [restriction enzymes, BamHI and HindIII; subtraction of ACI/N (ACI) amplicon from BUF/Nac (BUF) amplicon and vice versa] yielded 131 polymorphic markers; 125 of these markers were mapped to all chromosomes except for chromosome X. This was done by using a mapping panel of 105 ACI x BUF F2 rats. To complement the relative paucity of chromosomal markers in the rat, genetically directed RDA, which allows isolation of polymorphic markers in the specific chromosomal region, was performed. By changing the F2 driver-DNA allele frequency around the region, four markers were isolated from the D1Ncc1 locus. Twenty-five of 27 RDA markers were informative regarding the dot blot analysis of amplicons, hybridizing only with tester amplicons. Dot blot analysis at a high density per unit of area made it possible to process a large number of samples. Quantitative trait loci can now be mapped in the rat genome by processing a large number of samples with RDA markers and then by isolating markers close to the loci of interest by genetically directed RDA.


Subject(s)
Chromosome Mapping , Rats/genetics , Alleles , Animals , Blotting, Southern , Crosses, Genetic , DNA/isolation & purification , Deoxyribonuclease BamHI , Deoxyribonuclease HindIII , Electrophoresis, Agar Gel , Genetic Markers , Polymerase Chain Reaction , Rats/classification , Rats, Inbred ACI/genetics , Rats, Inbred BUF/genetics , Restriction Mapping
8.
Pathol Int ; 45(4): 261-5, 1995 Apr.
Article in English | MEDLINE | ID: mdl-7550994

ABSTRACT

In rats of the BUF/Mna strain epithelial thymoma development is regulated by a single autosomal susceptible gene, Tsr-1. In pre-thymoma stage, BUF/Mna rats have extremely large thymuses, when compared with those of other strains of rats. The large thymus size of this strain is contributed by a thymus-enlargement gene, Ten-1. On the other hand, reduced thymus size and suppression of thymoma development were found in heterozygous BUF/Mna-rnu/+ rats. Linkage studies between RNU and microsatellite and restriction fragment length polymorphism markers in ([BUF/Mna-rnu/rnu x WKY/NCrj] F1 x WKY/NCrj)- and (WKY/NCrj x [BUF/Mna-rnu/rnu x WKY/NCrj] F1)- backcross rats have led to the localization of RNU on chromosome 10. The rat homolog of mouse Mpo (myeloperoxidase) was also assigned to the chromosome 10. The gene order on the chromosome was MYHSE (myosin heavy chain of embryonic skeletal muscle)--(1.0 centimorgan [cM])--SHBG (sex hormone-binding globulin)--(4.0 cM)--RNU (Rowett rat nude)--(10.0 cM)--MPO--(13.0 cM)--AEP (anion exchange protein). Conserved linkage of homologous loci mapped to rat chromosome 10 and mouse chromosome 11 supports the hypothesis that the RNU and MPO loci are rat homologs of the mouse nu and Mpo loci.


Subject(s)
Genetic Linkage , Peroxidase/genetics , Rats, Inbred BUF/genetics , Rats, Nude/genetics , Animals , Crosses, Genetic , Female , Genes, Neoplasm , Genotype , Male , Rats , Thymoma/genetics
9.
J Neuroimmunol ; 52(2): 215-8, 1994 Jul.
Article in English | MEDLINE | ID: mdl-8034760

ABSTRACT

Inbred Buffalo rats (RT-1b) have been used in studies of experimental autoimmune encephalomyelitis and autoimmune thyroiditis. Since our studies, and those of others, have relied on the genetic purity of inbred Buffalo rats, we chose to test these animals for expression of strain-dependent, allotype-specific variants of CD45 (leukocyte common antigen, LCA) using the monoclonal antibodies RT7.1 and RT7.2. The goal of this study was to confirm the genetic purity and to verify the inbred status of Buffalo rats obtained from a commercial source.


Subject(s)
Genetic Variation , Leukocyte Common Antigens/genetics , Rats, Inbred BUF/genetics , Rats, Inbred BUF/immunology , Animals , Antibodies, Monoclonal , Female , Male , Rats , Rats, Inbred Lew
10.
Jpn J Cancer Res ; 84(8): 838-40, 1993 Aug.
Article in English | MEDLINE | ID: mdl-8407546

ABSTRACT

The thymoma-prone rat of the BUF/Mna strain is a useful model for human thymoma. In this strain thymoma development is regulated by a single autosomal susceptible gene, Tsr-1. At pre-thymoma age, BUF/Mna rats have extremely large thymuses, when compared to those of other strains of rats. Genetic studies in crosses between BUF/Mna rats with large thymuses and WKY/NCrj rats with small thymuses suggested the presence of a major autosomal gene, Ten-1, which contributes to thymus enlargement in a backcross population. Linkage studies between Ten-1 and microsatellite markers in backcross rats of (WKY/NCrj x BUF/Mna)F1 x BUF/Mna have led to the localization of Ten-1 in chromosome 1. This result may provide an approach to clone Tsr-1, which could be allelic to Ten-1.


Subject(s)
Chromosome Mapping , Rats, Inbred BUF/genetics , Rats, Inbred WKY/genetics , Thymus Gland/growth & development , Animals , Crosses, Genetic , Genetic Markers , Rats
11.
J Neuroimmunol ; 44(2): 215-9, 1993 May.
Article in English | MEDLINE | ID: mdl-8505411

ABSTRACT

The Lewis (LEW) rat strain is highly susceptible to a large number of experimentally induced inflammatory and autoimmune diseases. The Lewis resistant (LER) rat strain, which reportedly arose as a spontaneous mutation in a closed colony of LEW rats, is resistant to many of these disorders. The mechanism of resistance is not yet clear. We report the analysis of 19 simple dinucleotide repeat polymorphisms in 13 rat strains including the LEW/N and LER/N rat strains. The LEW/N and LER/N alleles were the same in only 42% of cases. For all of the other polymorphisms, the LER/N and Buffalo (BUF/N) rat strain alleles were identical. These data provide evidence that the LER strain did not arise as a spontaneous mutation in the LEW strain but is the result of an outcross between the LEW and BUF rat strains. The LER rat strain is now a recombinant inbred rat strain. This information should facilitate the genetic analysis of the loci responsible for resistance to experimental autoimmune disease in the LER rat.


Subject(s)
Autoimmune Diseases/genetics , Rats, Inbred Strains/genetics , Alleles , Animals , Autoimmune Diseases/immunology , Base Sequence , Crosses, Genetic , Immunity, Innate , Molecular Sequence Data , Oligodeoxyribonucleotides , Polymorphism, Genetic , Rats , Rats, Inbred ACI/genetics , Rats, Inbred BUF/genetics , Rats, Inbred F344/genetics , Rats, Inbred Lew/genetics , Rats, Inbred Strains/immunology , Repetitive Sequences, Nucleic Acid , Species Specificity
12.
Diabetes ; 41(12): 1617-23, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1446803

ABSTRACT

We describe the phenotypic characteristics of animals in the fifth backcross-intercross generation of a breeding program in which the RT1 u haplotype and the phenotypic trait responsible for the T-lymphopenia of BB rats have been transferred to the ACI background. In this generation of animals, 24% were lymphopenic with decreased numbers of PBL expressing CD5, TCR alpha, and RT6. The PBL of the lymphopenic animals had a decreased mitogenic response to ConA. All of the nonlymphopenic animals were homozygous for RT6.2. Phenotypic analysis of intestinal IEL revealed that this was also the case for the lymphopenic animals. Moreover, IEL of the lymphopenic animals exhibited a pattern of staining (increased numbers of TCR alpha beta+CD4+CD8+ and decreased numbers of TCR alpha beta+CD4-CD8+) similar to that of BB DP animals. The ACI.1U(BB)-lymphopenic animals, although having two of the genetic traits associated with the expression of spontaneous diabetes mellitus, uniformly fail to develop diabetes. Breeding studies in which these animals were crossed with BB and hBB rats suggest that other genes are necessary for development of overt diabetes.


Subject(s)
Diabetes Mellitus, Type 1/genetics , Lymphocytes/immunology , Major Histocompatibility Complex , Rats, Inbred BB/genetics , T-Lymphocyte Subsets/immunology , Animals , Antibodies, Monoclonal , CD4 Antigens/immunology , CD8 Antigens/immunology , Crosses, Genetic , DNA/genetics , DNA/isolation & purification , Diabetes Mellitus, Type 1/immunology , Disease Susceptibility/immunology , Female , Flow Cytometry , Genetic Predisposition to Disease , Haplotypes , Lymphocyte Activation , Male , Phenotype , Rats , Rats, Inbred BB/immunology , Rats, Inbred BUF/genetics , Rats, Inbred BUF/immunology , Receptors, Antigen, T-Cell, alpha-beta/immunology
14.
J Biol Chem ; 262(26): 12479-87, 1987 Sep 15.
Article in English | MEDLINE | ID: mdl-2442163

ABSTRACT

Functional and structural approaches were used to characterize the transcription units of the rat alpha-feto-protein (AFP) and albumin genes. A cell-free nuclear transcription assay and several genomic clones were used to show that: 1) the rate of transcription of these genes is closely related to the levels of corresponding mRNAs in the yolk sac and during rat liver development, indicating that the expression of the albumin and AFP genes is mainly regulated at the transcriptional level in the rat, and 2) the in vivo 5' end boundaries of the rat AFP and albumin transcription domains were mapped near the respective first exons. Due to the presence of repeated sequences, the 3' end boundary of both genes could not be accurately defined in the same manner. 3) No transcription could be detected until 7 kilobases upstream from the cap site of these genes. In addition, the organization of the rat AFP gene was analyzed by restriction endonuclease mapping, S1 nuclease mapping, and nucleotide sequencing. Our results indicate that: 1) the rat AFP gene is 20 kilobase pairs long and is split into 15 exons by 14 intervening sequences; 2) the transcription initiation site of the rat AFP gene is heterogenous; 3) the 5'-flanking region upstream from the rat AFP gene exhibits 60-90% similarity with the mouse and human AFP genes while no major nucleotide identity is found with the rat albumin gene; 4) a 90-base pair sequence present as one copy upstream from the rat and mouse AFP genes is present as two copies in the human genome; 5) several inverted repeats are mapped in the 5'-flanking region indicating potential stem-loop structures. One highly conserved structure encompasses an enhancer-like core sequence and the sequence recognized by the TGGCA-binding protein.


Subject(s)
Albumins/genetics , Promoter Regions, Genetic , Rats, Inbred Strains/genetics , alpha-Fetoproteins/genetics , Age Factors , Animals , Base Sequence , Genes , Nucleic Acid Conformation , Rats , Rats, Inbred BUF/genetics , Rats, Inbred Strains/growth & development , Transcription, Genetic
15.
Nucleic Acids Res ; 15(16): 6419-36, 1987 Aug 25.
Article in English | MEDLINE | ID: mdl-3306601

ABSTRACT

Rat genomic regions covering c-myc were cloned from the DNA of both normal liver and two lines of Morris hepatomas, one of which had c-myc amplification. The three restriction maps showed perfect agreement within the overlapping regions. The 7 kb regions, which included the entire normal rat c-myc and the region 2.2 kb upstream, and one from the hepatomas, were sequenced and found to be identical. The coding regions of exons 2 and 3 were highly conserved between rat, mouse and man, but some differences in amino acids were noted. Exon 1 and the non-coding region of exon 3 showed limited homology between the three species. Rat exon 1 contained several nonsense codons in each frame and no ATG codon, indicating there to be no coding capacity in this exon. The 2.2 kb upstream regions and the introns compared showed unusual conservation between the rat and human genes. Some motifs, previously proposed as having a functional role in human c-myc, were also found in equivalent positions of the rat sequence. Nucleas S1 protection mapping revealed the second promoter to be preferentially used in most tissues or in hepatoma cells, and the second poly A addition signal to be the only one functional in all the RNA sources examined.


Subject(s)
Proto-Oncogene Proteins/genetics , Proto-Oncogenes , Rats/genetics , Amino Acid Sequence , Animals , Base Sequence , DNA, Neoplasm/genetics , DNA, Recombinant , Gene Amplification , Genes , Humans , Liver/analysis , Liver Neoplasms, Experimental/analysis , Mice/genetics , Promoter Regions, Genetic , Proto-Oncogene Proteins c-myc , Rats, Inbred BUF/genetics , Sequence Homology, Nucleic Acid , Species Specificity
17.
Ann N Y Acad Sci ; 475: 66-80, 1986.
Article in English | MEDLINE | ID: mdl-3538975

ABSTRACT

It has been hypothesized that autoimmune disease may result from a derangement of the idiotype-anti-idiotype network. However, the evidence in favor of a role of anti-idiotypic immunity in autoimmunity is still scarce. For this reason, we have investigated animal models of autoimmune thyroiditis and glomerulonephritis, addressing the following questions: Are autoimmune responses idiotypically heterogeneous? Are auto-anti-idiotypic antibodies detectable in autoimmunity? Is it possible to demonstrate quantitative or qualitative changes in idiotypic and anti-idiotypic lymphocytes during the course of autoimmune disease? To date, results obtained in our laboratory may be summarized as follows: Cross-reacting idiotypes were present on human and animal autoantibodies; Circulating auto-anti-idiotypic antibodies were not detected in any of the models studied; Changes in idiotypic and anti-idiotypic lymphocytes were observed in animals with autoimmune disease.


Subject(s)
Autoantibodies/immunology , Autoimmune Diseases/immunology , Disease Models, Animal/immunology , Glomerulonephritis/immunology , Immunoglobulin Idiotypes/immunology , Rats, Inbred BN/immunology , Rats, Inbred BUF/immunology , Rats, Inbred Strains/immunology , Thyroiditis, Autoimmune/immunology , Thyroiditis/immunology , Animals , Antibodies, Anti-Idiotypic/immunology , Glomerulonephritis/genetics , Humans , Rats , Rats, Inbred BN/genetics , Rats, Inbred BUF/genetics , Rodent Diseases/genetics , Rodent Diseases/immunology , Thyroiditis/genetics
18.
Genetics ; 108(3): 633-49, 1984 Nov.
Article in English | MEDLINE | ID: mdl-6149973

ABSTRACT

Phenylethanolamine N-methyltransferase (PNMT) is the enzyme that catalyzes the S-adenosyl-L-methionine-dependent methylation of (-)norepinephrine to (-)epinephrine in the adrenal medulla. Adrenal PNMT activity is markedly different in two highly inbred rat strains; enzyme activity in the F344 strain is more than fivefold greater than that in the Buf strain. Initial characterization of the enzyme in the two inbred strains reveals evidence for catalytic and structural differences, as reflected in dissimilar Km values for the cosubstrate (S-adenosyl-L-methionine) and prominent differences in thermal inactivation curves. To assess adrenal PNMT activity in an F344 X Buf pedigree, we employed a statistical procedure to test for one- and two-locus hypotheses in the presence of within-class correlations due to cage or litter effects. The PNMT data in the pedigree are best accounted for by segregation at a simple major locus superimposed upon a polygenic background; data obtained from the biochemical studies suggest that the major locus is a structural gene locus.


Subject(s)
Adrenal Medulla/enzymology , Phenylethanolamine N-Methyltransferase/genetics , Rats, Inbred BUF/genetics , Rats, Inbred F344/genetics , Rats, Inbred Strains/genetics , Animals , Catecholamines/analysis , Crosses, Genetic , Dopamine beta-Hydroxylase/analysis , Female , Genes , Male , Rats , Tyrosine 3-Monooxygenase/analysis
19.
Tumour Biol ; 5(6): 365-70, 1984.
Article in English | MEDLINE | ID: mdl-6085601

ABSTRACT

Restriction endonuclease digestion using Hind III and Msp I and Southern blot analysis of DNA from the liver of three inbred rat strains and one outbred strain using cDNA probes yields two banding patterns for the alphafetoprotein and albumin genes. Buffalo and Fischer DNA have one pattern whereas ACI had a different pattern for both genes. Sprague Dawley DNA contains fragments of both patterns suggesting heterozygosity in some individuals of this strain. These polymorphisms do not appear to be associated with any structural or biological differences in the proteins resulting from expression of these genes.


Subject(s)
Albumins/genetics , Rats/genetics , alpha-Fetoproteins/genetics , Animals , DNA/analysis , Male , Polymorphism, Genetic , Rats, Inbred ACI/genetics , Rats, Inbred BUF/genetics , Rats, Inbred F344/genetics , Rats, Inbred Strains/genetics
20.
Mol Gen Genet ; 195(1-2): 153-8, 1984.
Article in English | MEDLINE | ID: mdl-6208454

ABSTRACT

Two structural variants of the rat alpha-fetoprotein (AFP) gene have been detected in different inbred strains of rats by EcoRI or HindIII restriction enzyme cleavage of cellular DNA, agarose gel electrophoresis and Southern blot hybridization using 32P-labeled cloned rat AFP cDNA probes. The type I AFP gene variant is characteristic of the Sprague-Dawley strain, and type II is found in Buffalo rats. These variants appear to represent two different allelic forms of the rat AFP gene since they are inherited in a normal Mendelian fashion when Sprague-Dawley and Buffalo rats are crossed. The mapping results suggest that the two allelic variants differ from each other by multiple cleavage site variations (base pair substitutions) and by an insertion or deletion of DNA sequences. An extensive sequence variation appears to exist between the two forms of the rat AFP gene; we have estimated that as much as 2.7% of the nucleotides in this region vary between the two alleles.


Subject(s)
Genes , Genetic Variation , Rats, Inbred Strains/genetics , alpha-Fetoproteins/genetics , Animals , DNA Restriction Enzymes , Male , Nucleic Acid Hybridization , Rats , Rats, Inbred BUF/genetics , Rats, Inbred Lew/genetics
SELECTION OF CITATIONS
SEARCH DETAIL
...