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PubMed2000

Inherited variability of the mitochondrial genome and successful aging in humans.

Increasing data indicate that polymorphic variants of nuclear loci can affect rate and quality of aging in humans. However, the mitochondrial genome is another good candidate, because of the central role played by mitochondrial genes in oxidative phosphorylation (OXPHOS) and cell metabolism. A characteristic of the mitochondrial genome (mtDNA) is the high level of interindividual variability that ensues from high mutation rate and unilinear inheritance. Related groups of germline/inherited mtDNA polymorphisms (haplogroups) have been identified as continent-specific sets of stable/ancient/associated restriction fragment length polymorphisms in the mtDNA coding region, representing markers capable of exactly depicting the mtDNA pool of a specific population. The hypothesis can be put forward that mtDNA variants included in a haplogroup may have similar OXPHOS efficiency and therefore act as genetic factors predisposing to individual successful or unsuccessful aging. This idea can be explored by sampling groups of individuals of different ages from a well-defined population and comparing the pools of mtDNA haplogroups between samples. The results obtained by screening mtDNA haplogroups in about 800 Italians of different ages, including more than 200 centenarians, agree with the hypothesis that the inherited variability of the mitochondrial genome is associated with the chance of successful aging and longevity in humans.

Aging↗
PubMed1988

Inherited progressive spinal myelinopathy in Murray Grey cattle.

In a breeding experiment conducted to determine the mode of inheritance of progressive spinal myelinopathy, semen from a Murray Grey bull which had previously sired affected calves was used to inseminate 120 cows. Female progeny were then inseminated with semen from the same bull. Of the 51 calves born, six (11.8%) had spinal cord lesions consistent with progressive spinal myelinopathy. From analysis of pedigrees and the results of the breeding experiment it was concluded that the condition was inherited as an autosomal recessive condition in Murray Grey cattle.

Animals↗
PubMed1990

Inherited epidermal dysplasia in Holstein-Friesian calves.

Inherited epidermal dysplasia (IED), formerly called baldy calf syndrome, is a lethal disease of calves of Holstein-Friesian ancestry. The disease causes progressive illthrift and skin, horn and hoof lesions, which can be confused with inherited zinc deficiency. The clinicopathological features and ancestry of 10 affected calves in Gippsland, Victoria are described.

Animals↗
PubMed1996

Inherited disorders: the comparative picture.

When confronted with a novel familial disorder, veterinarians should consult McKusick's catalogue of inherited disorders in humans, called Mendelian Inheritance in Man (MIM), or its online version (OMIM), to see whether a similar disorder has been reported in humans. They should also consult the other readily available sources of comparative information on mice and domesticated species. Increasingly, such consultations can be conducted on the Internet via the World Wide Web. If it is thought that an animal disorder is homologous with a human disorder, publications describing the animal disorder should include the MIM number(s) for that disorder. Future research can then test the hypothesis of homology, until a consensus is reached.

Animals↗
PubMed1999

Polycystic kidney disease in bull terriers: an autosomal dominant inherited disorder.

The prevalence, mode of inheritance and urinalysis findings in Bull Terriers with polycystic kidney disease were assessed by screening 150 clinically normal dogs. The disorder was diagnosed in 39 dogs on the basis of renal ultrasound results and family history of the disease. In equivocal cases confirmation required gross and histopathological renal examination. Necropsy was performed on nine affected dogs and the kidneys from another five affected animals were also examined. Renal cysts were usually bilateral, occurred in cortex and medulla and varied from less than 1 mm to over 2.5 cm in diameter. Cysts were lined by epithelial cells of nephron origin. Abnormal urine sediment and proteinuria were common in affected dogs. The disease appears to be inherited in a highly penetrant autosomal dominant manner.

Animals↗
PubMed1992

Juvenile cataract with autosomal recessive inheritance. A study from the Aland Islands, Finland.

Juvenile (including congenital and infantile) cataract occurs commonly as part of a more generalized or systematic condition, or as a component of a syndrome. Isolated juvenile cataract is a relatively rare disorder and the mode of inheritance is often autosomal dominant. Autosomal recessive transmission of isolated juvenile cataract is rare. The present paper is a report of 15 cases of juvenile cataract on the Aland Islands (Finland) with about 23,000 inhabitants. Twelve belong to 7 sibships of two different pedigrees and 3 cases are sporadic, of which we have found no genealogical connections in the last 6-10 generations to the two cataracta pedigrees. One of the sporadic cases presented an operated cleft palate and a chromosomal anomaly. In another sporadic case the mother probably had been infected with rubella during early gestation. In the third sporadic case the cataract was combined with partial aniridia, but he has several genealogical connections to one of the cataract pedigrees. Consanguinity between the parents was detected in 5 of the 7 sibships, in some even on various ancestral levels. Apart from the cataracts, all patients were healthy, with normal intellect, behavior, hearing, growth and development. They were neurologically intact and there were no ocular lesions apart from cataract. In the Alandic familial cases the cataracts appear to be an autosomal recessive trait. A family branch originating from southwestern Sweden and south Norway showed transmission of the cataract in three successive generations. The possibility of quasi-dominant inheritance is discussed against the background that autosomal recessive juvenile cataract may not be so rare as the small number of recorded cases would suggest.(ABSTRACT TRUNCATED AT 250 WORDS)

Aged↗
PubMed2003

Asymmetric inheritance of oxidatively damaged proteins during cytokinesis.

Carbonylated proteins were visualized in single cells of the budding yeast Saccharomyces cerevisiae, revealing that they accumulate with replicative age. Furthermore, carbonylated proteins were not inherited by daughter cells during cytokinesis. Mother cells of a yeast strain lacking the sir2 gene, a life-span determinant, failed to retain oxidatively damaged proteins during cytokinesis. These findings suggest that a genetically determined, Sir2p-dependent asymmetric inheritance of oxidatively damaged proteins may contribute to free-radical defense and the fitness of newborn cells.

Actins↗
PubMed1966

Inheritance of reacitivity to experimental manipulation in mice.

The mode of inheritance of open-field defecation was found to differ according to earlier treatment of the mice. Activity of hybrids, however, was closer to that of the less active parent for all conditions of pretreatment. These results suggest that adequate sampling not only of gene pools, but also of both pretest and test environments, is necessary before statements concerning effects of prior treatment, or mode of inheritance of specific behavior, are valid.

Animals↗
PubMed1966

Inherited variations of human serum alpha-1-antitrypsin.

The normal serum alpha(1)-antitrypsin migrates as a three banded patternwhen separated electrophoretically in starch gel with a sodium acetateethylenediaminetetraacetic acid buffer of pH 4.95. The results obtained when certain inherited variants of the serum alpha(1)-antitrypsin are separated electrophoretically suggest that the previously described variations in the region preceding the albumin band represent inherited variations of the serum alpha(1)-antitrypsin.

Blood Protein Electrophoresis↗
PubMed1991

Heteroplasmy suggests limited biparental inheritance of Mytilus mitochondrial DNA.

Strict maternal inheritance of mitochondrial DNA is commonly observed in animals. There is usually only one mitochondrial DNA population (homoplasmy) within an individual. Mussels of the Mytilus edulis species group appear to be exceptions in both respects. Of 150 Mytilus individuals examined, 85 were heteroplasmic. Mitochondrial DNA types within heteroplasmic individuals differed greatly; in one comparison, the inferred sequence difference was 20 +/- 5 percent. Homoplasmic individuals with mitochondrial DNA similar to the heteroplasmic mitochondrial DNA types were found. These observations are best explained by the hypothesis that biparental inheritance of mitochondrial DNA can occur in Mytilus.

Animals↗
PubMed1996

Support for the prion hypothesis for inheritance of a phenotypic trait in yeast.

A cytoplasmically inherited genetic element in yeast, [PSI+], was confirmed to be a prionlike aggregate of the cellular protein Sup35 by differential centrifugation analysis and microscopic localization of a Sup35-green fluorescent protein fusion. Aggregation depended on the intracellular concentration and functional state of the chaperone protein Hsp104 in the same manner as did [PSI+] inheritance. The amino-terminal and carboxy-terminal domains of Sup35 contributed to the unusual behavior of [PSI+]. [PSI+] altered the conformational state of newly synthesized prion proteins, inducing them to aggregate as well, thus fulfilling a major tenet of the prion hypothesis.

Amino Acid Sequence↗
PubMed1999

Inheritance of resistance to bacillus thuringiensis toxin (Dipel ES) in the european corn borer

Resistance in the European corn borer, Ostrinia nubilalis (Hubner), to a commercial formulation of Bacillus thuringiensis (Bt) Berliner toxin, Dipel ES, appears to be inherited as an incompletely dominant autosomal gene. This contrasts with the inheritance of resistance to Bt in other insects, where it has usually been characterized as a recessive trait. The proposed high-dose/refuge strategy for resistance management in Bt maize depends on resistance being recessive or partially recessive. If field resistance turns out to be similar to this laboratory resistance, the usefulness of the high-dose/refuge strategy for resistance management in Bt maize may be diminished.

Journal Article↗
PubMed1988

Deficit of spinal cord glycine/strychnine receptors in inherited myoclonus of Poll Hereford calves.

Inherited myoclonus of Poll Hereford calves is characterized by hyperesthesia and myoclonic jerks of the skeletal musculature, which occur spontaneously and in response to sensory stimuli. The disease shows autosomal recessive inheritance, and significant proportions of the Poll Hereford herds in many countries are thought to be carriers of the mutant gene. Studies revealed a specific and marked (90 to 95 percent) deficit in [3H]strychnine binding sites in spinal cord membranes from myoclonic animals compared to controls, reflecting a loss of, or defect in, glycine/strychnine receptors. Spinal cord synaptosomes prepared from affected animals showed a significantly increased ability to accumulate [3H]glycine, indicating an increased capacity of the high-affinity neuronal uptake system for glycine. In contrast, stimulus-induced glycine release and spinal cord glycine concentrations were unaltered.

Amino Acids↗
PubMed2000

Genetic requirements for inheritance of RNAi in C. elegans.

In Caenorhabditis elegans, the introduction of double-stranded RNA triggers sequence-specific genetic interference (RNAi) that is transmitted to offspring. The inheritance properties associated with this phenomenon were examined. Transmission of the interference effect occurred through a dominant extragenic agent. The wild-type activities of the RNAi pathway genes rde-1 and rde-4 were required for the formation of this interfering agent but were not needed for interference thereafter. In contrast, the rde-2 and mut-7 genes were required downstream for interference. These findings provide evidence for germ line transmission of an extragenic sequence-specific silencing factor and implicate rde-1 and rde-4 in the formation of the inherited agent.

Animals↗
PubMed2000

An inherited functional circadian clock in zebrafish embryos.

Circadian clocks are time-keeping systems found in most organisms. In zebrafish, expression of the clock gene Period3 (Per3) oscillates throughout embryogenesis in the central nervous system and the retina. Per3 rhythmic expression was free-running and was reset by light but not by the developmental delays caused by low temperature. The time of fertilization had no effect on Per3 expression. Per3 messenger RNA accumulates rhythmically in oocytes and persists in embryos. Our results establish that the circadian clock functions during early embryogenesis in zebrafish. Inheritance of maternal clock gene products suggests a mechanism of phase inheritance through ovogenesis.

Amino Acid Sequence↗
PubMed2000

Multigenerational cortical inheritance of the Rax2 protein in orienting polarity and division in yeast.

Diploid yeast cells repeatedly polarize and bud from their poles, probably because of highly stable marks of unknown composition. Here, Rax2, a membrane protein, was shown to behave as such a mark. The Rax2 protein itself was inherited immutably at the cell cortex for multiple generations, and Rax2 was shown to have a half-life exceeding several generations. The persistent inheritance of cortical protein markers would provide a means to couple a cell's history to the future development of a precise morphogenetic form.

Cell Division↗
PubMed1978

Inherited medullary thyroid carcinoma: a final monoclonal mutation in one of multiple clones of susceptible cells.

Inherited medullary thyroid carcinomas contain one form of glucose-6-phosphate dehydrogenase (G6PD) in black female patients who are mosaic in normal tissues for G6PD types A and B. The same individual may have several tumors each containing either G6PD A or G6PD B. The data suggest that the inherited defect is an initial mutation producing multiple clones of defective cells; each tumor then arises as a final mutation in one clone of these cells.

Black People↗
PubMed1976

Clonal origin of inherited medullary thyroid carcinoma and pheochromocytoma.

A black female with inherited medullary thyroid carcinoma and pheochromocytoma was a mosaic for glucose-6-phosphate dehydrogenase types A and B in normal tissues (blood, thyroid, and adrenal gland); both the medullary carcinoma and pheochromocytoma tissue showed a B pattern only. This finding suggests a single clone origin for each of the tumors. Other inherited tumors similarly studied in man have appeared to be multiclonal in origin.

Adult↗