Heat Shock Protein Hsp70 Gene Research Articles

Comparative Analysis of Heat Shock Protein Genes Hsp70 and Hsp90 Expression by Live and Killed Edwardsiella tarda Challenge in Rohu, Labeo rohita

Comparative Analysis of Heat Shock Protein Genes Hsp70 and Hsp90 Expression by Live and Killed Edwardsiella tarda Challenge in Rohu, Labeo rohita

128 Additional dietary DL-methionine affects tissue redox and inflammation status of broiler chicks in response to high stocking density

Abstract We determined if 30% extra supplemental DL-methionine affected oxidative and inflammatory responses of broilers stocked at a high density. A total of 560 day-old male Cornish cockerel chicks were divided into 4 groups: 2 stocking densities (2.9 and 3.8 kg/ft2) and 2 methionine supplementations (grower: 2.90 or 3.77 g/kg and finisher: 2.60 or 3.38 g/kg). Chicks were fed the same corn-soy starter diet and then respective experimental diets (grower: 6.4 g SAA/kg, finisher: 5.9 g SAA/kg, n = 10 pens/treatment). Blood and tissues (3 chicks/pen) were sampled at the end of each period. Data were analyzed by two-way ANOVA. The high density elevated (P < 0.05) glutathione concentration in the plasma, breast, and thigh of growers, but decreased (P < 0.05) it in the liver of growers and thigh of finishers. The high methionine elevated (P < 0.05) glutathione concentration in the thigh at both ages. There were interactions (P < 0.05) between dietary methionine and stocking density on activities of antioxidant enzymes including GST in 2 or more tissues at both ages and GPX and SOD in the thigh of growers. Hepatic expression of inflammation-related gene IL-6 was decreased (P < 0.05) by the high density, while heat shock protein genes HSP70 and HSP90 were decreased (P < 0.05) by the high methionine. Expression of stress-related genes TNFα and JNK was decreased (P < 0.05) by a combined high methionine and density treatment. The high methionine decreased (P < 0.05) finisher thigh and breast malondialdehyde concentrations and grower plasma glucose concentrations. Neither the density nor the methionine supplementation affected concentrations of plasma ferric reducing ability, serum amyloid A, and corticosterone or hepatic protein carbonyl. In conclusion, the high stocking density showed bilateral effects on the redox and inflammatory responses of broilers. Supplemental extra methionine modulated some of those effects.

Gene expression during the intra-puparial stage of Chrysomya megacephala: Implications for postmortem interval estimation

Abstract Chrysomya megacephala (Fabricius, 1794) (Diptera: Calliphoridae) is one of the most predominant calliphorid species which arrives and colonizes a cadaver first in its native range of the Australian and Oriental regions, and the intra-puparial stage of this species accounts for about half of its immature stage. Therefore, establishing a reliable aging method of the intra-puparial stage of C. megacephala is very important to accurately estimate the minimum postmortem interval (PMImin). In this study, actin was used as an internal reference gene to study the expression of three genes, ecdysone receptor gene ecr, white-eye gene white, and heat shock protein gene hsp70, at different time points during intra-puparial development of C. megacephala. Quantification through real-time PCR revealed that these genes can be used to age the intra-puparial period of C. megacephala as they exhibit regular changes and gene expression level was temperature-dependent. The overall gene expression profile of ecr showed a downward trend throughout the intra-puparial stage. White expression increased steadily until it peaked when intra-puparial development reached 45%, and the expression began to decrease when the intra-puparial development reached 55%. hsp70 was first down-regulated at 0–15% of intra-puparial development, and then slightly up-regulated at 15–40%, and finally down-regulated again until the end of intra-puparial development. This study provides molecular indicators of age during the intra-puparial stage of C. megacephala, and combining gene expression with the morphological methods can lead to more accurate estimation for PMImin.

Computational Characterization of the mtORF of Pocilloporid Corals: Insights into Protein Structure and Function in Stylophora Lineages from Contrasting Environments.

More than a decade ago, a new mitochondrial Open Reading Frame (mtORF) was discovered in corals of the family Pocilloporidae and has been used since then as an effective barcode for these corals. Recently, mtORF sequencing revealed the existence of two differentiated Stylophora lineages occurring in sympatry along the environmental gradient of the Red Sea (18.5 °C to 33.9 °C). In the endemic Red Sea lineage RS_LinB, the mtORF and the heat shock protein gene hsp70 uncovered similar phylogeographic patterns strongly correlated with environmental variations. This suggests that the mtORF too might be involved in thermal adaptation. Here, we used computational analyses to explore the features and putative function of this mtORF. In particular, we tested the likelihood that this gene encodes a functional protein and whether it may play a role in adaptation. Analyses of full mitogenomes showed that the mtORF originated in the common ancestor of Madracis and other pocilloporids, and that it encodes a transmembrane protein differing in length and domain architecture among genera. Homology-based annotation and the relative conservation of metal-binding sites revealed traces of an ancient hydrolase catalytic activity. Furthermore, signals of pervasive purifying selection, lack of stop codons in 1830 sequences analyzed, and a codon-usage bias similar to that of other mitochondrial genes indicate that the protein is functional, i.e., not a pseudogene. Other features, such as intrinsically disordered regions, tandem repeats, and signals of positive selection particularly in Stylophora RS_LinB populations, are consistent with a role of the mtORF in adaptive responses to environmental changes.

Ecologically Relevant Temperature Ramping Rates Enhance the Protective Heat Shock Response in an Intertidal Ectotherm.

Thermal stress experiments are essential for understanding organisms' thermal limits and the physiological processes that contribute to establishing those limits. Experiments typically employ either an abrupt transfer to near-lethal temperatures or a gradually increasing thermal exposure. In the current study, we used three populations of the intertidal copepod Tigriopus californicus that are known to differ in upper thermal tolerance to investigate the effects of gradual versus abrupt thermal exposures on survivorship, developmental time, and heat shock protein gene expression. The developmental rate of nauplii was unaffected following the gradual exposure, whereas developmental time slowed by ∼2 d (∼20%) following an abrupt exposure. The gradual exposure also improved survivorship in comparison to the abrupt exposure. Furthermore, the heat shock protein genes hsp70 and hspb1 showed greater upregulation during the gradual thermal exposure compared to the abrupt exposure. Though the differences in response to each thermal regime varied in magnitude among the different populations, the types of responses were very similar (i.e., following the gradual exposure survivorship increased, developmental time showed no effect, and heat shock protein gene upregulation during the exposure increased). Therefore, the enhanced protective effect of the heat shock response during gradual exposures appears to be conserved within the species despite population-level differences in thermal tolerance. Thus, an ecologically relevant thermal exposure likely enables improved cellular protective mechanisms by allowing for an effective and timely heat shock response, which plays a role in mitigating the effects of thermal stress and thereby enhances tolerance to elevated temperatures.

Reference gene selection and evaluation for expression analysis using qRT-PCR in Galeruca daurica (Joannis).

Quantitative real-time PCR (qRT-PCR) has been used extensively to analyze gene expression and decipher gene function. To obtain the optimal and stable normalization factors for qRT-PCR, selection and validation of reference genes should be conducted in diverse conditions. In insects, more and more studies confirmed the necessity and importance of reference gene selection. In this study, eight traditionally used reference genes in Galeruca daurica (Joannis) were assessed, using qRT-PCR, for suitability as normalization genes under different experimental conditions using four statistical programs: geNorm, Normfinder, BestKeeper and the comparative ΔC t method. The genes were ranked from the most stable to the least stable using RefFinder. The optimal suite of recommended reference genes was as follows: succinate dehydrogenase (SDHA) and tubulin-alpha (TUB-α) for temperature-treated larvae; ribosomal protein L32, SDHA and glutathione S-transferase were best for all developmental stages; ACT and TUB-α for male and female adults; SDHA and TUB-α were relatively stable and expressed in different tissues, both diapause and non-diapause adults. Reference gene evaluation was validated using expression of two target genes: the P450 CYP6 gene and the heat shock protein gene Hsp70. These results confirm the importance of custom reference gene selection when studies are conducted under diverse experimental conditions. A standardized qRT-PCR analysis procedure for gene functional studies is provided that could be useful in studies on other insect species.

The regulation of thermal stress induced apoptosis in corals reveals high similarities in gene expression and function to higher animals.

Recent studies suggest that controlled apoptotic response provides an essential mechanism, enabling corals to respond to global warming and ocean acidification. However, the molecules involved and their functions are still unclear. To better characterize the apoptotic response in basal metazoans, we studied the expression profiles of selected genes that encode for putative pro- and anti-apoptotic mediators in the coral Stylophora pistillata under thermal stress and bleaching conditions. Upon thermal stress, as attested by the elevation of the heat-shock protein gene HSP70’s mRNA levels, the expression of all studied genes, including caspase, Bcl-2, Bax, APAF-1 and BI-1, peaked at 6–24 h of thermal stress (hts) and declined at 72 hts. Adversely, the expression levels of the survivin gene showed a shifted pattern, with elevation at 48–72 hts and a return to basal levels at 168 hts. Overall, we show the quantitative anti-apoptotic traits of the coral Bcl-2 protein, which resemble those of its mammalian counterpart. Altogether, our results highlight the similarities between apoptotic networks operating in simple metazoans and in higher animals and clearly demonstrate the activation of pro-cell survival regulators at early stages of the apoptotic response, contributing to the decline of apoptosis and the acclimation to chronic stress.

Analysis of survival, gene expression and behavior following chill-coma in the medfly Ceratitis capitata: Effects of population heterogeneity and age

The medfly Ceratitis capitata is an agricultural pest distributed worldwide thanks, in part, to its phenotypic plasticity of thermal tolerance. Cold exposure has been shown to reduce C. capitata survival, which may affect its distribution in areas with subfreezing temperatures. When insects are increasingly cooled, they attain a critical thermal threshold and enter a chill-coma state characterized by cessation of movement. It is not clear how a rapid cold exposure affects the physiological state of medflies, and how this is influenced by age and population heterogeneity. In order to approach these questions, C. capitata single-sex laboratory populations of 15 and 30days old were subjected to a chill-coma recovery assay, and separated according to their recovery time in three subgroups: Fast-Subgroups, Intermediate-Subgroups, and Slow-Subgroups. Thereafter, we analyzed their survival, behavioral, and gene expression outputs. In female and old male populations, we found that flies with the slowest recovery time had a reduced life expectancy, a higher initial mortality rate, and a worse climbing performance compared with flies that recovered faster. Therefore, we were able to separate subgroups that developed chilling-injury from subgroups that had a reversible full recovery after cold exposure. The gene expression analysis of the heat shock protein genes hsp70 and hsp83 showed no clear association with the parameters studied. Interestingly, thorax expression levels of the Cu/Zn superoxide dismutase gene were elevated during the recovery phase in the Fast-Subgroups, but remained constant in the Slow-Subgroups that developed chilling-injury. On the other hand, none of the young male subgroups seemed to have suffered irreversible damage. Thus, we concluded that depending on age and population heterogeneity, chill-coma recovery time points out significant differences on individual cold tolerance. Moreover, the inability to properly induce the antioxidant defense system to counteract the oxidative damage caused by cold seems to contribute to the development of chilling-injury.

Correction: Compound A, a Selective Glucocorticoid Receptor Modulator, Enhances Heat Shock Protein Hsp70 Gene Promoter Activation

Correction: Compound A, a Selective Glucocorticoid Receptor Modulator, Enhances Heat Shock Protein Hsp70 Gene Promoter Activation

Compound A, a Selective Glucocorticoid Receptor Modulator, Enhances Heat Shock Protein Hsp70 Gene Promoter Activation

Compound A possesses glucocorticoid receptor (GR)-dependent anti-inflammatory properties. Just like classical GR ligands, Compound A can repress NF-κB-mediated gene expression. However, the monomeric Compound A-activated GR is unable to trigger glucocorticoid response element-regulated gene expression. The heat shock response potently activates heat shock factor 1 (HSF1), upregulates Hsp70, a known GR chaperone, and also modulates various aspects of inflammation. We found that the selective GR modulator Compound A and heat shock trigger similar cellular effects in A549 lung epithelial cells. With regard to their anti-inflammatory mechanism, heat shock and Compound A are both able to reduce TNF-stimulated IκBα degradation and NF-κB p65 nuclear translocation. We established an interaction between Compound A-activated GR and Hsp70, but remarkably, although the presence of the Hsp70 chaperone as such appears pivotal for the Compound A-mediated inflammatory gene repression, subsequent novel Hsp70 protein synthesis is uncoupled from an observed CpdA-induced Hsp70 mRNA upregulation and hence obsolete in mediating CpdA’s anti-inflammatory effect. The lack of a Compound A-induced increase in Hsp70 protein levels in A549 cells is not mediated by a rapid proteasomal degradation of Hsp70 or by a Compound A-induced general block on translation. Similar to heat shock, Compound A can upregulate transcription of Hsp70 genes in various cell lines and BALB/c mice. Interestingly, whereas Compound A-dependent Hsp70 promoter activation is GR-dependent but HSF1-independent, heat shock-induced Hsp70 expression alternatively occurs in a GR-independent and HSF1-dependent manner in A549 lung epithelial cells.

Ocean Acidification at High Latitudes: Potential Effects on Functioning of the Antarctic Bivalve Laternula elliptica

Ocean acidification is a well recognised threat to marine ecosystems. High latitude regions are predicted to be particularly affected due to cold waters and naturally low carbonate saturation levels. This is of concern for organisms utilising calcium carbonate (CaCO3) to generate shells or skeletons. Studies of potential effects of future levels of pCO2 on high latitude calcifiers are at present limited, and there is little understanding of their potential to acclimate to these changes. We describe a laboratory experiment to compare physiological and metabolic responses of a key benthic bivalve, Laternula elliptica, at pCO2 levels of their natural environment (430 µatm, pH 7.99; based on field measurements) with those predicted for 2100 (735 µatm, pH 7.78) and glacial levels (187 µatm, pH 8.32). Adult L. elliptica basal metabolism (oxygen consumption rates) and heat shock protein HSP70 gene expression levels increased in response both to lowering and elevation of pH. Expression of chitin synthase (CHS), a key enzyme involved in synthesis of bivalve shells, was significantly up-regulated in individuals at pH 7.78, indicating L. elliptica were working harder to calcify in seawater undersaturated in aragonite (ΩAr = 0.71), the CaCO3 polymorph of which their shells are comprised. The different response variables were influenced by pH in differing ways, highlighting the importance of assessing a variety of factors to determine the likely impact of pH change. In combination, the results indicate a negative effect of ocean acidification on whole-organism functioning of L. elliptica over relatively short terms (weeks-months) that may be energetically difficult to maintain over longer time periods. Importantly, however, the observed changes in L. elliptica CHS gene expression provides evidence for biological control over the shell formation process, which may enable some degree of adaptation or acclimation to future ocean acidification scenarios.

Alterations of HSP70 gene expression in rainbow trout (Oncorhyncus mykiss) exposed to deltamethrin

The aim of the study was to assess the effects of deltamethrin, a synthetic pyrethroid pesticide and potential toxic pollutant to aquatic ecosystems, on the heat shock protein HSP70 gene expression in rainbow trout. Deltamethrin was applied at 0.3 and 0.6 \mug/L for 28 days under laboratory conditions. After the experiment, HSP70 was amplified for 20-40 PCR cycles for the control and deltamethrin-treated fish groups. While the quantitative mRNA level was low in the 40^t^h PCR cycle in the control, it was higher in the fish exposed to deltamethrin. The differences between the treated groups and the control group were statistically significant (P < 0.01), but the difference between the treatment groups was not.

Mechanisms of plant adaptation/memory in rice seedlings under arsenic and heat stress: expression of heat-shock protein gene HSP70

Plants can withstand many abiotic stresses. Stress adaptation through retention of imprints of previous stress exposure has also been described in plants. We have characterized the imprint or memory of adaptive stress responses of rice seedlings to arsenic (As) and heat stress. Two-week-old rice seedlings (both with and without As) were given a 45 °C heat shock for 3 h. While under heat shock, the leafy portion of the seedlings was harvested at regular intervals. Subsequently, the seedlings were kept at room temperature for recovery and sampling continued over 3 h. Total RNA and protein were extracted from the leafy portion of the seedlings and complementary DNA (cDNA) was prepared from total RNA. The cDNA was used as a template for the polymerase chain reaction to identify the transcription level of HSP70. Protein extracted from the seedlings was western-blotted. HSP70 and actin (loading control) antibodies were used to recognize the proteins on the same blot. Our studies reveal that HSP70, a cellular chaperone gene, is over-expressed at the mRNA and protein levels when rice seedlings are exposed to As and heat. The effect is cumulative and increases with the duration of stress for 3 h. During 3 h recovery from heat stress at ambient temperatures for 3 h, the chaperone remains expressed at higher levels in plants pre-exposed to As. Our findings demonstrate a retention of the imprint of previous stress exposure, perhaps through sustained activation of the signalling pathways upstream of over-expression of HSP70. Furthermore, stress-induced HSP70 expression was additive/cumulative for continued exposure to similar or different kinds of stress, indicating that a commonality of signal transduction networks is adopted when plants experience more than one stress.

Use of primers based on the heat shock protein genes hsp70, hsp40, and hsp10, for the detection of bovine mastitis pathogens Streptococcus agalactiae, Streptococcus uberis and Streptococcus bovis

Streptococcus agalactiae, Streptococcus uberis, and Streptococcus bovis are three of the major pathogens which cause mastitis in dairy herds. Since conventional methods for the detection of these mastitis pathogens are laborious and time-consuming, rapid methods are needed. With an attempt to know if heat shock protein (HSP) genes other than HSP60 gene, could be used for PCR primer designing, in this study, we tried to design PCR primers based on the heat shock protein genes hsp70, hsp40, and hsp10 for the specific detection of S. agalactiae, S. uberis, and S. bovis, respectively. Using these primers, all the randomly selected target strains could be specifically detected. Bacterial species other than the target organisms, including strains of other Streptococcus spp., and strains of non- Streptococcus spp., would not generate any false positive results. As these PCR primers were used for direct detection of mastitis pathogens, the detection limit was N ( N = 1–9) × 10 3 CFU/ml of cell dilutions. If a 10 h pre-enrichment step was performed, the detection limit was N × 10 0 CFU/ml. Thus, these primers could be used for the specific and sensitive detection of bovine mastitis bacteria.

Early Onset of Heat-Shock Response in Mouse Embryos Revealed by Quantification of Stress-Induciblehsp70iRNA

Heat shock response is fully established in mouse embryos at the blastocyst stage, but it is unclear when this response first arises during development. To shed light on this question, we used a single-tube method to quantify mRNA levels of the heat shock protein genes hsp70.1 and hsp70.3 ( hsp70i) in individual cleavage-stage embryos that had or had not been heat-shocked. While untreated, healthy embryos contained very low copy numbers of hsp70i RNA, heat shock rapidly induced the synthesis of hundreds of hsp70i transcripts per blastomere at both the 4-cell and the 8-cell stages. In addition, we performed hsp70i measurements in embryos that had not been heat-shocked but had been very slow in developing. Quantification of hsp70i RNA and genomic DNA copy numbers in these slow-growing embryos demonstrated the presence of two distinct populations. Some of the embryos contained considerable levels of hsp70i RNA, a finding consistent with the hypothesis of endogenous metabolic stress accompanied by cell cycle arrest and delayed development. Other slow-growing embryos contained no hsp70i RNA and fewer than expected hsp70i gene copies, suggesting the possibility of ongoing apoptosis. In conclusion, this study demonstrates that mouse embryos can activate hsp70i expression in response to sub-lethal levels of stress as early as at the 4-cell stage. Our results also indicate that quantification of hsp70i DNA and RNA copy numbers may provide a diagnostic tool for embryonic health.

Genetics of human longevity with emphasis on the relevance of HSP70 as candidate genes

Human longevity is determined to a certain extent by genetic factors. Several candidate genes have been studied for their association with human longevity, but the data collected so far are inconclusive. One of the reasons is the choice of the candidate genes in addition to the choice of an appropriate study design and methodology. Since aging is characterized by a progressive accumulation of molecular damage and an attenuation of the cellular defense mechanisms, the focus of studies on human longevity association with genes has now shifted to the pathways of cellular maintenance and repair mechanisms. One such pathway includes the battery of stress response genes, especially the heat shock protein HSP70 genes. Three such genes, HSPA1A, HSPA1B and HSPA1L, are present within the MHC-III region on the short arm of chromosome 6. We and others have found alleles, genotypes and haplotypes which have been significantly associated with human longevity and survival. We have also provided some functional evidence for these genetic associations by showing that isolated peripheral blood cells from those genotypes which are negatively associated with human longevity also have less ability to respond to heat shock. Stress response genes, particularly HSP70, are now the major candidates in the gene-longevity association studies.

Cloning and characterization of the executioner caspases 3, 6, 7 and Hsp70 in hyperthermic Atlantic salmon ( Salmo salar) embryos

Hyperthermia during embryogenesis has been reported to induce deformities in Atlantic salmon ( Salmo salar). To examine the involvement of executioner caspases in hyperthermia-induced cell-death in a poikilotherm vertebrate species, five genes encoding caspase-3,-6, and -7 were cloned from Atlantic salmon, and the expression was studied in thermal stressed salmon embryos. The salmon genome contained two genetically distinct variants of both salmon caspase-3 and caspase-6 that is likely the result of two independent chromosome or genome duplications. Whereas only partial caspase-3A encoding sequences were isolated, the full-length caspase-3B cDNA encodes the inactive proenzyme of 279 amino acids (aa) consisting of an N-terminal prodomain and the large and the small subunit. The salmon caspase-6A and caspase-6B proenzymes include an additional linker region between the two subunits. The deduced salmon caspase-7 consists of only 245 aa and lacks the prodomain and part of the large subunit similar to the predicted caspase-7 of the puffer fish Tetraodon sp.. Increased apoptotic activity as evidenced by cleavage of nuclear DNA was demonstrated in salmon embryos incubated at 18–20 °C for 84 h after acclimatization at 8 °C. Hyperthermia-induced activation of the executioner caspases was indicated by the increased mRNA levels of caspase-3B, caspase-6A/B and caspase-7 after 54 h heat exposure as quantified by real-time RT-PCR. The 2–2.5 fold increase in the mRNA expression of the heat shock protein Hsp70 gene coincided with the peak mRNA values of the executioner caspases. Whole-mount in situ hybridization of the salmon embryo identified caspase-7 mRNA in the lens exclusively, while caspase-3B and caspase-6A/B were expressed in multiple tissues of exposed and control embryos. Interestingly, cardiac expression of caspase-6A/B was only identified in heat stressed embryos . Altogether, these results shed light on evolutionary aspects of the executioner caspases in vertebrates and their expression in salmon embryos exposed to hyperthermia. In particular, the heat sensitive caspase-6 expression in the embryonic heart is of interest since cardiac malformations are an emergent problem in salmon aquaculture.

584. Gene Delivery to Primary Neuronal Cells

Top of pageAbstract Neuronal protection under numerous clinical circumstances (i.e. trauma brain injury, stroke, ischemia and circulation arrested surgery, etc.) remains a tough challenge due to the paucity of effective clinical options. Transient gene delivery to CNS neuronal cells may offer an alternative approach to induce neuronal protection. We have previously shown widespread distribution, uptake, and expression in rat brain after non-viral, cationic lipid-mediated delivery of reporter gene vectors to the lateral ventricle 1,2. In order to further develop techniques for, and understand the mechanisms of, non-viral gene delivery, we conducted cationic lipid mediated gene delivery of fire fly luciferase mRNA and DNA to primary rat cortical cells to study the post-transfection transgene expression profiles. The delivery of mRNA resulted in a rapid onset of luciferase expression 1 hour after transfection, peaked at 5- 6 hours post transfection, and diminished to base line 12 hours after transfection. Compared to the delivery of mRNA, DNA delivery resulted in a much later onset of gene expression. Although the transgene expression after DNA delivery was generally one order of magnitude higher than after mRNA delivery, the earliest significant luciferase activity after DNA transfection did not appear until 7 hours after transfection. Peak expression following DNA delivery was 36-48 hours after transfection, and transgene expression persisted at a significant level for at least one week before it dropped to base line. Based on this observation, we attempted the delivery of mRNA and DNA vectors that encode for the heat shock protein gene HSP70. The inducible HSP70 is a chaperone protein and its expression has protective effects under stress conditions. HSP70 was delivered using non-viral cationic lipid-mediated techniques that we have developed to rat primary cortical cells, and analyzed by flow cytometry and immunohistochemistry. Consistent with the luciferase activity results, we detected evenly stained HSP70 expression 5 hours after the delivery of HSP70 mRNA, while expression after the delivery of HSP70 DNA appeared to peak at 36-48 hours.

Human heat shock protein gene polymorphisms and sudden infant death syndrome.

Comparison of the frequency of occurrence of restriction fragment length polymorphisms in control human DNAs and DNAs from infants dying from sudden infant death syndrome has indicated no significant difference in the case of restriction fragment length polymorphisms associated with the heat shock protein genes hsp70 and hsp90. A highly significant difference was detected, however, in the case of the specific restriction fragment length polymorphisms detected by an hsp60 gene probe in MspI digests.

Restriction fragment length polymorphisms at the heat shock protein HSP70 gene(s) in pigs.

Pigs from a population consisting of eight US breeds or strains and three Chinese breeds were examined by restriction fragment length polymorphism (RFLP) analysis of the heat shock protein HSP70 gene(s). Limited polymorphisms with PstI and PvuII restriction enzymes were observed, but there were no polymorphisms with BamHI and BglI.