ABSTRACT
The SP/KLF transcription factor family contains over 25 members sharing a DNA-binding domain composed of three zinc fingers of the C(2)H(2) type. We previously identified the sixth member of the SP subfamily (Sp6). The 5' end of the Sp6 transcript was not cloned and was predicted bioinformatically. A mouse molar tooth cDNA was then isolated differing from the Sp6 sequence by its 5' end, and was named epiprofin. Sp6 and epiprofin are currently used as synonyms. Here, we show that the Sp6 transcript possesses a first exon distinct from the epiprofin one: the Sp6 gene thus uses two promoters, generating two transcript variants which differ in their first exon. Furthermore, we identified an Sp6 opposite strand transcript (Sp6os) and examined, by quantitative RT-PCR experiments, the presence and the abundance of these two transcripts in mouse tissues. We also mapped the mouse locus by FISH to chromosome 11D.
Subject(s)
Kruppel-Like Transcription Factors/genetics , Promoter Regions, Genetic/genetics , RNA, Antisense/genetics , Animals , Base Sequence , Gene Expression , Gene Expression Profiling , In Situ Hybridization, Fluorescence , Male , Mice , Mice, Inbred Strains , Molecular Sequence Data , Physical Chromosome Mapping , RNA, Messenger/genetics , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Transcription Factors/genetics , Transcription Initiation SiteABSTRACT
The neural mechanisms controlling mate recognition and heterosexual partner preference are sexually differentiated by perinatal actions of sex steroid hormones. We previously showed that the most important action of oestrogen during prenatal development is to defeminise and, to some extent, masculinise brain and behaviour in mice. Female mice deficient in alpha-foetoprotein (AFP) due to a targeted mutation in the Afp gene (AFP-KO) do not show any female sexual behaviour when paired with an active male because they lack the protective action of AFP against maternal oestrogens. In the present study, we investigated whether odour preferences, another sexually differentiated trait in mice, are also defeminised and/or masculinised in AFP-KO females due to their prenatal exposure to oestrogens. AFP-KO females of two background strains (CD1 and C57Bl/6j) preferred to investigate male over female odours when given the choice between these two odour stimuli in a Y-maze, and thus remained very female-like in this regard. Thus, the absence of lordosis behaviour in these females cannot be explained by a reduced motivation of AFP-KO females to investigate male-derived odours. Furthermore, the presence of a strong male-directed odour preference in AFP-KO females suggests a postnatal contribution of oestrogens to the development of preferences to investigate opposite-sex odours.
Subject(s)
Estrogens/physiology , Mating Preference, Animal/physiology , Prenatal Exposure Delayed Effects , Smell/physiology , alpha-Fetoproteins/physiology , Analysis of Variance , Animals , Choice Behavior , Female , Mice , Mice, Inbred C57BL , Mice, Knockout , Pregnancy , Sex Differentiation/physiology , alpha-Fetoproteins/geneticsABSTRACT
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.
Subject(s)
Calcium-Binding Proteins/genetics , Chromosome Mapping/methods , Computational Biology/methods , Eye Proteins/genetics , Fatty Acid-Binding Proteins/genetics , Genes/genetics , Interleukin-13 Receptor alpha1 Subunit/genetics , Membrane Glycoproteins/genetics , Nerve Tissue Proteins/genetics , Receptor, EphB4/genetics , Receptors, Cytoplasmic and Nuclear/genetics , Receptors, Peptide/genetics , Ribosomal Proteins/genetics , Animals , Carrier Proteins/genetics , Databases, Genetic , Genome , Hybrid Cells , Mice , Rats , Sequence Analysis, DNAABSTRACT
This work shows that the proximal promoter of the mouse Afp gene contains a Ku binding site and that Ku binding is associated with down-regulation of the transcriptional activity of the Afp promoter. The Ku binding site is located in a segment able to adopt a peculiar structured form, probably a hairpin structure. Interestingly, the structured form eliminates the binding sites of the positive transcription factor HNF1. Furthermore, a DNAse hypersensitive site is detected in footprinting experiments done with extracts of AFP non-expressing hepatoma cells. These observations suggest that the structured form is stabilised by Ku and is associated with extinction of the gene in AFP non-expressing hepatic cells.
Subject(s)
Antigens, Nuclear/metabolism , DNA-Binding Proteins/metabolism , DNA/chemistry , Gene Expression Regulation , Promoter Regions, Genetic , alpha-Fetoproteins/genetics , Animals , Base Sequence , Binding Sites , Cell Line, Tumor , DNA/metabolism , Hepatocyte Nuclear Factor 1 , Humans , Ku Autoantigen , Mice , Molecular Sequence Data , Nucleic Acid Conformation , Rats , alpha-Fetoproteins/metabolismABSTRACT
Ammonium excretion into urine is a major process essential to the regulation of acid-base homeostasis. We have shown that Rh-type proteins, including renal RhCG, belong to the Mep/Amt family of ammonium transporters and promote bi-directional ammonium transport upon heterologous expression in yeast. To study the physiological role of RhCG and to test a potential function in ammonium excretion, we have generated mice bearing an invalidation of the corresponding gene.
Subject(s)
Cation Transport Proteins/physiology , Membrane Glycoproteins/physiology , Quaternary Ammonium Compounds/metabolism , Acidosis/metabolism , Animals , Blood Proteins/genetics , Blood Proteins/metabolism , Cation Transport Proteins/biosynthesis , Cation Transport Proteins/deficiency , Cation Transport Proteins/genetics , Cation Transport Proteins/metabolism , Glycoproteins/metabolism , Humans , Ion Transport , Kidney/metabolism , Liver/metabolism , Membrane Glycoproteins/biosynthesis , Membrane Glycoproteins/deficiency , Membrane Glycoproteins/genetics , Membrane Glycoproteins/metabolism , Membrane Transport Proteins/metabolism , Mice , Mice, Knockout , Multigene Family , Rats , Recombinant Fusion Proteins/metabolism , Saccharomyces cerevisiae/metabolismABSTRACT
Most cancers are genetically complex and heterogeneous, a serious obstacle to identifying specific genes underlying the disease. If inbred animal models are used, then both the genetic constitution and environmental influences can be carefully controlled. Females of the BDII inbred rat strain are genetically predisposed to endometrial cancer; more than 90% of virgin BDII females will develop endometrial adenocarcinoma (EAC) during their life span. BDII females were crossed to males from inbred strains with low EAC incidence (SPRD or BN). When F(1) males were backcrossed to BDII females to generate N(1) populations of offspring, about one fourth of the female progeny developed EAC. With transmission disequilibrium test analysis, significant association was detected in three chromosomal regions (on RNO1, RNO11, and RNO17) in the SPRD crosses and in the short arm of RNO20 in the BN crosses. It appears that several susceptibility genes with minor but cooperating effects are responsible for the susceptibility. Furthermore, it seems clear from the interstrain crosses not only that the onset of tumors depends on the presence of susceptibility alleles from the EAC-prone BDII strain, but also that tumor development is affected by the contribution of a genetic component derived from the nonsusceptible strains.
Subject(s)
Adenocarcinoma/genetics , Disease Models, Animal , Endometrial Neoplasms/genetics , Genetic Predisposition to Disease , Adenocarcinoma/pathology , Animals , Chromosome Mapping , Crosses, Genetic , Cytogenetic Analysis , DNA, Neoplasm/analysis , Disease Susceptibility , Endometrial Neoplasms/pathology , Female , Genetic Markers , Male , Microsatellite Repeats , Rats , Rats, Inbred StrainsABSTRACT
Comparative mapping between the rat and mouse genomes has shown that some chromosomes are entirely or almost entirely conserved with respect to gene content. Such is the case of rat chromosome 11 (RNO11) and mouse chromosome 16 (MMU16). We determined to what extent such an extensive conservation of synteny is associated with a conserved gene order. Therefore, we regionally localized several genes on RNO11. The comparison of the gene map of RNO11 and MMU16 unambiguously shows that the gene order has not been conserved in the Murinae lineage, thereby implying the occurrence of intrachromosomal evolutionary rearrangements. The transition from one chromosome configuration to the other one can be explained either by two intrachromosomal recombinations or by a single intrachromosomal recombination accompanied by neocentromere emergence.
Subject(s)
Chromosomes, Mammalian/genetics , Conserved Sequence/genetics , Evolution, Molecular , Gene Order/genetics , Gene Rearrangement/genetics , Synteny/genetics , Animals , Chromosome Mapping/methods , Genome , Mice , RatsABSTRACT
ODF2 (outer dense fiber 2) was first described as the main protein component of the sperm tail cytoskeleton, the outer dense fibers, but was shown recently to be a component of the centrosomal scaffold in chicken. In mouse two related ODF2 cDNA clones were isolated which have been suggested to be most likely the result of alternative splicing. We show here the exon/intron organisation of mouse ODF2 and demonstrate that alternative splicing results in related cDNA sequences and most likely explains, at least partially, the highly complex protein pattern detected on Western blots. ODF2 was mapped to rat chromosome 3 and more specifically by FISH analysis at bands 3q11-->3q12. In addition, we demonstrate that ODF2 is indeed a component of the centrosome and the mitotic spindle poles in mammals.
Subject(s)
Centrosome/chemistry , Cytoskeletal Proteins/genetics , Heat-Shock Proteins/genetics , Animals , Base Sequence , COS Cells , Chlorocebus aethiops , Chromosome Mapping , Cytoskeletal Proteins/analysis , Exons , Genome , Heat-Shock Proteins/analysis , Introns , Male , Mice , Molecular Sequence Data , NIH 3T3 Cells , Rats , Sperm Tail/chemistry , Spindle Apparatus/chemistryABSTRACT
There are clear indications that inheritance plays an essential role in certain cases of human endometrial cancer, and there are at least 2 forms of early-onset heritable endometrial adenocarcinomas (EACs). Females of the BDII inbred rat strain are known to be genetically predisposed to endometrial carcinoma, and we have performed a genetic analysis of susceptibility to endometrial cancer in this strain. F(2) populations were generated by crossing BDII females with males from 2 different strains with a low incidence of EAC, and the occurrence of endometrial cancer was studied. Three chromosome regions associated to EAC susceptibility were identified, and the susceptibility genes in these regions were designated Ecs1, Ecs2 and Ecs3. Our results indicate that the genes affecting susceptibility to EAC are different in the 2 crosses, suggesting that the genes behind the susceptibility in BDII animals may interact with different genes in different genetic backgrounds.
Subject(s)
Adenocarcinoma/genetics , Endometrial Neoplasms/genetics , Genetic Predisposition to Disease , Alleles , Animals , Female , Genetic Linkage , Genotype , RatsSubject(s)
Cell Cycle Proteins , DNA-Binding Proteins/genetics , Genes, Tumor Suppressor , In Situ Hybridization, Fluorescence , RNA-Binding Proteins/genetics , Radiation Hybrid Mapping , Rats/genetics , Transcription Factors , Adenoma/genetics , Animals , Chromosomes, Human, Pair 20/genetics , Chromosomes, Human, Pair 6/genetics , Chromosomes, Human, Pair 8/genetics , Humans , Tumor Suppressor ProteinsABSTRACT
The glypicans compose a family of glycosylphosphatidylinositol (GPI)-anchored heparan sulfate proteoglycans that play a role in the control of cell division and growth regulation. So far, six members (GPC1-6) of this family are known in vertebrates. The rat glypican gene 3 (Gpc3) was previously assigned to chromosome Xq36 (Shen et al., 1997). Using standard and radiation cell hybrids, we localized the five other rat glypican genes.
Subject(s)
Heparan Sulfate Proteoglycans/genetics , Radiation Hybrid Mapping , Animals , Chromosomes/genetics , Cloning, Molecular , Expressed Sequence Tags , Mice , RatsABSTRACT
We established a radiation hybrid (RH) map of several genes and anonymous markers in the lower half of rat chromosome 2, a chromosome region that contains quantitative trait loci (QTLs) for blood pressure, diabetes and inflammatory response. Two of the newly localized genes (Crh and Il6r) encode proteins involved in the regulation of inflammatory and immune events. Our data show that they reside within regions that were genetically defined as QTLs controlling the inflammatory response. These genes are thus both functional and positional candidates.
Subject(s)
Corticotropin-Releasing Hormone/genetics , Inflammation/genetics , Quantitative Trait, Heritable , Radiation Hybrid Mapping , Receptors, Interleukin-6/genetics , Animals , Genes , Genetic Markers , In Situ Hybridization, Fluorescence , Lod Score , Rats , SoftwareABSTRACT
The rat strain COP is resistant to spontaneous and carcinogen-induced mammary cancer, whereas the strain WF is susceptible. Using genetic linkage analysis of (WF x COP) F1 x WF backcrosses, LC Hsu, LA Shepel and co-workers showed that a region at the centromeric end of Chromosome (Chr) 2 (2q1) segregates with the sensitivity to mammary cancer development. The responsible locus was named Mcs1 (for mammary cancer susceptibility 1). We have developed the chromosome map of the 2q1 region by localizing 18 genes, 4 ESTs, and several anonymous markers, using radiation hybrids and fluorescence in situ hybridization. The region containing Mcs1 was delineated to 2q12-q14. Five of the genes (Mef2c, Map1b, Ccnh, Rasa, Rasgrf2) were assigned to this region and were shown to be expressed in the rat mammary glands, while three possible functional candidate genes, Pi3kr1, Rad17, and Naip, were excluded from the critical region. Since cyclin H, encoded by Ccnh, plays an important role in the control of the cell cycle and since the proteins encoded by Rasa and Rasgrf2 control the activity of the RAS oncoprotein, the corresponding genes appeared as both functional and positional Mcs1 candidates. RT-PCR experiments on RNA extracted from mammary glands of the two rat strains (COP, WF) was done. No amino acid sequence difference was found between the two strains. These results argue against the hypothesis that any of these three genes is Mcs1.
Subject(s)
Mammary Neoplasms, Experimental/genetics , Animals , Base Sequence , DNA, Complementary , Expressed Sequence Tags , Humans , Immunity, Innate/genetics , Mice , Molecular Sequence Data , Mutagenesis , RatsABSTRACT
BACKGROUND: Fischer 344 (F344) rats are relatively resistant to hypoxia-induced right ventricular (RV) hypertrophy compared with the Wistar-Kyoto (WKY) strain. These 2 strains were used to examine the genetic basis for the differential response. METHODS AND RESULTS: Male F(2) offspring from an F344xWKY intercross were exposed to hypoxia (10% O(2)) for 3 weeks, and pulmonary artery pressure and cardiac chamber weights were measured. Genomic DNA was screened by use of polymorphic microsatellite markers across the whole genome (excluding the sex chromosomes). A quantitative trait locus (QTL) for RV weight was identified on rat chromosome 17 (lod score 6.5) that accounted for 22% of the total variance of RV weight in the F(2) population and was independent of pulmonary artery pressure. The peak was centered over marker D17Rat41, close to Chrm3, with a 1-lod support interval of 5 cM. Comparison of homologous regions in mice and humans suggested that Ryr2, the cardiac isoform of the ryanodine receptor, colocalizes with our QTL. A panel of somatic cell hybrids and fluorescence in situ hybridization mapped Ryr2 close to the gene Chrm3 within our QTL. [(3)H]Ryanodine binding to cardiac membranes from the parental strains showed a 21% reduction in B(max) in the WKY compared with the F344 strain, with no difference in K:(d). CONCLUSIONS: These data provide the first demonstration of a QTL linked to the RV response to hypoxia-induced pulmonary hypertension. The Ryr2 receptor gene lies within this QTL and merits further investigation as a candidate for this differential RV response.
Subject(s)
Hypertension, Pulmonary/complications , Hypertrophy, Right Ventricular/complications , Ryanodine Receptor Calcium Release Channel/genetics , Animals , Body Weight , Chromosomes, Human, Pair 17 , Crosses, Genetic , Genetic Linkage , Humans , Hypertension, Pulmonary/etiology , Hypertension, Pulmonary/genetics , Hypertrophy, Right Ventricular/genetics , Hypoxia , In Situ Hybridization, Fluorescence , Male , Myocardium/metabolism , Organ Size , Phenotype , Quantitative Trait, Heritable , Radioligand Assay , Rats , Rats, Inbred F344 , Rats, Inbred WKY , Ryanodine Receptor Calcium Release Channel/metabolismABSTRACT
Using the sequence of the SP1 zinc-finger DNA-binding domain as a probe to screen a mouse EST database, we identified two novel members of the SP/XKLF transcription factor family, KLF13 and KLF14. The mouse Klf13 cDNA (1310 bp in length) contains a single open reading frame of 288 amino acids with a DNA-binding domain closely related to that of the human RFLAT-1 protein and a putative transactivator N-terminal domain rich in proline and alanine residues. The mouse Klf13 gene seems to be the homologue of the human RFLAT1 gene. The mouse Klf14 sequence is homologous to a human genomic sequence from chromosome 17 that is believed to code for a protein with three zinc fingers at the end of its C-terminal domain. Using reverse transcription-polymerase chain reaction, we showed ubiquitous expression of Klf13 and Klf14 in adult mice. A third member of this family was also identified in a human EST database; this sequence was found to be identical to KLF11 (TIEG2), recently identified by Cook et al. (1998, J. Biol. Chem. 273: 25929-25936). The corresponding mouse cDNA was isolated and sequenced. The three genes were localized in the human and the rat: chromosomes 15 (human KLF13), 17q21.3-q22 (human KLF14; HGMW-approved symbol SP6), and 2p25 (human KLF11) and chromosomes 1q31-q32 (rat Klf13), 10q31-q32.1 (rat Klf14) (SP6), and 6q16-q21 (rat Klf11).
Subject(s)
Multigene Family , Trans-Activators/genetics , Transcription Factors/genetics , Zinc Fingers , Amino Acid Sequence , Animals , Apoptosis Regulatory Proteins , Base Sequence , Cell Cycle Proteins/genetics , Chromosome Mapping , Chromosomes, Human, Pair 15 , Expressed Sequence Tags , Humans , Kruppel-Like Transcription Factors , Mice , Molecular Sequence Data , Rats , Repressor Proteins/genetics , Sequence Homology, Amino Acid , Sp Transcription Factors , Trans-Activators/classification , Transcription Factors/classificationABSTRACT
In order to improve the rat gene map and comparative mapping with the human and the mouse, we determined the chromosome localization of 54 rat genes. Most genes encode transcription factors or other regulatory proteins of cancer relevance. The human homologs of four genes were also assigned to their respective chromosome. These data generated anchor points between the recently established radiation hybrid maps and the genetic and cytogenetic maps. They improve comparative mapping between the rat, the mouse, and the human gene maps, and in particular they disclose four new synteny groups conserved in the rat and the human. These new localizations should also be useful for the identification of genes involved in the control of quantitative traits such as cancer susceptibility or diabetes.