Genetic polymorphism of human serum ribonuclease I (RNase I).

Abstract:

:One of the human urinary ribonucleases (RNases) was isolated and purified to homogeneity (SDS-PAGE) by means of a series of column chromatographies. The enzyme, designated RNase 1, is a glycoprotein with a molecular weight of approximately 16,000. Rabbit antibody to the purified RNase 1 reacted with human urine and sera, as well as with the purified RNase 1. The genetic polymorphism of serum RNase 1 was studied by polyacrylamide gel isoelectric focusing (IEF-PAGE) in a pH range of 5-8, followed by immunoblotting with antisera specific for RNase 1. Two common phenotypes, RNASE1 1 and RNASE1 1-2, were easily recognized. The homogeneous phenotype, RNASE1 1, consisted of four major bands with different pI values, and the heterogeneous phenotype, RNASE1 1-2, was presumed to represent a mixture of each of the homogeneous phenotypes 1 and 2; however, the other homogeneous phenotype, RNASE1 2, was not detected in our samples. Family studies are in agreement with an autosomal codominant transmission of the two alleles. Population studies indicate that the frequencies of the RNASE 1 and RNASE1 2 alleles are .988 and .012, respectively.

journal_name

Am J Hum Genet

authors

Yasuda T,Sato W,Mizuta K,Kishi K

subject

Has Abstract

pub_date

1988-04-01 00:00:00

pages

608-14

issue

4

eissn

0002-9297

issn

1537-6605

journal_volume

42

pub_type

杂志文章
  • Mitochondrial DNA polymorphism among five Asian populations.

    abstract::Mitochondrial DNA (mtDNA) polymorphisms were detected using 13 restriction enzymes on the total DNA obtained from blood samples of five Asian populations: Japanese and Ainu of northern Japan, Korean, Negrito (Aeta) of the Philippines, and Vedda of Sri Lanka. Of a total of 28 restriction-enzyme morphs detected, eight h...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Harihara S,Saitou N,Hirai M,Gojobori T,Park KS,Misawa S,Ellepola SB,Ishida T,Omoto K

    更新日期:1988-08-01 00:00:00

  • Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.

    abstract::CHARGE syndrome is a well-established multiple-malformation syndrome with distinctive consensus diagnostic criteria. Characteristic associated anomalies include ocular coloboma, choanal atresia, cranial nerve defects, distinctive external and inner ear abnormalities, hearing loss, cardiovascular malformations, urogeni...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/500273

    authors: Lalani SR,Safiullah AM,Fernbach SD,Harutyunyan KG,Thaller C,Peterson LE,McPherson JD,Gibbs RA,White LD,Hefner M,Davenport SL,Graham JM,Bacino CA,Glass NL,Towbin JA,Craigen WJ,Neish SR,Lin AE,Belmont JW

    更新日期:2006-02-01 00:00:00

  • Parental trisomy 21 mosaicism.

    abstract::A family with three children with trisomy 21 in which the mother is a phenotypically normal, trisomy 21/normal mosaic was studied. Chromosome 21 fluorescent heteromorphisms were used to document that two of the three number 21's in two of the Down syndrome offspring were of maternal origin. Five cytogenetic surveys in...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Harris DJ,Begleiter ML,Chamberlin J,Hankins L,Magenis RE

    更新日期:1982-01-01 00:00:00

  • Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease.

    abstract::Perrault syndrome is a genetically and clinically heterogeneous autosomal-recessive condition characterized by sensorineural hearing loss and ovarian failure. By a combination of linkage analysis, homozygosity mapping, and exome sequencing in three families, we identified mutations in CLPP as the likely cause of this ...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2013.02.013

    authors: Jenkinson EM,Rehman AU,Walsh T,Clayton-Smith J,Lee K,Morell RJ,Drummond MC,Khan SN,Naeem MA,Rauf B,Billington N,Schultz JM,Urquhart JE,Lee MK,Berry A,Hanley NA,Mehta S,Cilliers D,Clayton PE,Kingston H,Smith MJ,W

    更新日期:2013-04-04 00:00:00

  • Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure.

    abstract::Premature ovarian failure (POF) is characterized by elevated gonadotropins and amenorrhea in women aged <40 years. In a Lebanese family with five sisters who received the diagnosis of POF, we established linkage to the long arm of the X chromosome (between Xq21.1 and Xq21.3.3), using whole-genome SNP typing and homozy...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/505406

    authors: Lacombe A,Lee H,Zahed L,Choucair M,Muller JM,Nelson SF,Salameh W,Vilain E

    更新日期:2006-07-01 00:00:00

  • Cowden syndrome-affected patients with PTEN promoter mutations demonstrate abnormal protein translation.

    abstract::Germline mutations of PTEN (phosphatase and tensin homolog deleted on chromosome 10) are associated with the multihamartomatous disorder Cowden syndrome (CS). Moreover, patients with CS with germline PTEN promoter mutations have aberrant PTEN protein expression and an increased frequency of breast cancer. Here, we exa...

    journal_title:American journal of human genetics

    pub_type: 杂志文章,多中心研究

    doi:10.1086/521051

    authors: Teresi RE,Zbuk KM,Pezzolesi MG,Waite KA,Eng C

    更新日期:2007-10-01 00:00:00

  • Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.

    abstract::The disease classification neurodegeneration with brain iron accumulation (NBIA) comprises a clinically and genetically heterogeneous group of progressive neurodegenerative disorders characterized by brain iron deposits in the basal ganglia. For about half of the cases, the molecular basis is currently unknown. We use...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2011.09.007

    authors: Hartig MB,Iuso A,Haack T,Kmiec T,Jurkiewicz E,Heim K,Roeber S,Tarabin V,Dusi S,Krajewska-Walasek M,Jozwiak S,Hempel M,Winkelmann J,Elstner M,Oexle K,Klopstock T,Mueller-Felber W,Gasser T,Trenkwalder C,Tiranti V,Kr

    更新日期:2011-10-07 00:00:00

  • Analysis of three restriction fragment length polymorphisms in the human type II procollagen gene.

    abstract::Cloned genomic DNA sequences corresponding to various regions of the human type II procollagen gene were used to analyze the DNA from 78 normal volunteers. Southern hybridization experiments detected polymorphic HindIII, BamHI, and EcoRI sites. The presence of the polymorphic HindIII site results in a 7.0-kilobase (kb...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Eng CE,Strom CM

    更新日期:1985-07-01 00:00:00

  • Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

    abstract::We devised a rapid PCR-based method to screen for an A----G transition at nucleotide 8344 of the human mitochondrial tRNA(Lys) gene, which was recently reported, by Shoffner and co-workers, to be associated with myoclonus epilepsy and ragged-red fibers (MERRF), a maternally transmitted mitochondrial encephalomyopathy ...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Zeviani M,Amati P,Bresolin N,Antozzi C,Piccolo G,Toscano A,DiDonato S

    更新日期:1991-02-01 00:00:00

  • The presence of two different infantile Tay-Sachs disease mutations in a Cajun population.

    abstract::A study was undertaken to characterize the mutation(s) responsible for Tay-Sachs disease (TSD) in a Cajun population in southwest Louisiana and to identify the origins of these mutations. Eleven of 12 infantile TSD alleles examined in six families had the beta-hexosaminidase A (Hex A) alpha-subunit exon 11 insertion m...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: McDowell GA,Mules EH,Fabacher P,Shapira E,Blitzer MG

    更新日期:1992-11-01 00:00:00

  • The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease.

    abstract::The chromosome 19 apolipoprotein E/CI/CII gene cluster was examined for evidence of linkage to a familial Alzheimer disease (FAD) locus. The family groups studied were Volga German (VG), early-onset non-VG (ENVG; mean age at onset < 60 years), and late-onset families. A genetic association was observed between apolipo...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Yu CE,Payami H,Olson JM,Boehnke M,Wijsman EM,Orr HT,Kukull WA,Goddard KA,Nemens E,White JA

    更新日期:1994-04-01 00:00:00

  • Cytogenetic and molecular analysis of sex-chromosome monosomy.

    abstract::X chromosome- and Y chromosome-specific DNA probes were used to study different aspects of the genesis of sex-chromosome monosomy. Using X-linked RFLPs, we studied the parental origin of the single X chromosome in 35 spontaneously aborted and five live-born 45,X conceptions. We determined the origin in 35 cases; 28 ha...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Hassold T,Benham F,Leppert M

    更新日期:1988-04-01 00:00:00

  • Sandhoff disease heterozygote detection: a component of population screening for Tay-Sachs disease carriers. I. Statistical methods.

    abstract::Serum and leukocyte hexosaminidase profiles (total activity and percent heat-labile activity levels) in obligate Sandhoff disease (SHD) heterozygotes differ from those of obligate Tay-Sachs disease (TSD) heterozygotes and noncarrier individuals. We have developed a procedure to identify, with 95% sensitivity, carriers...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Cantor RM,Lim JS,Roy C,Kaback MM

    更新日期:1985-09-01 00:00:00

  • The first arrival time and mean age of a deleterious mutant gene in a finite population.

    abstract::The mean and standard deviation of the first arrival time for a single mutant to reach a certain frequency and the mean age of a mutant persisting in a population have been studied using diffusion methods. These quantities are shown to be highly dependent on both the heterozygous effect and the population size. For pa...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Li WH

    更新日期:1975-05-01 00:00:00

  • Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.

    abstract::Supernumerary marker chromosomes (SMCs) of chromosome 15, designated "SMC(15)s," are the most common SMC in humans, accounting for as much as 60% of all those observed. We report the characterization of 46 large SMC(15)s, using both fluorescence in situ hybridization and polymerase chain reaction analysis within and d...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/379155

    authors: Roberts SE,Maggouta F,Thomas NS,Jacobs PA,Crolla JA

    更新日期:2003-11-01 00:00:00

  • Microsatellite polymorphism in the heme oxygenase-1 gene promoter is associated with susceptibility to emphysema.

    abstract::Cigarette smoke, containing reactive oxygen species, is the most important risk factor for chronic pulmonary emphysema (CPE). Heme oxygenase-1 (HO-1) plays a protective role as an antioxidant in the lung. A (GT)n dinucleotide repeat in the 5'-flanking region of human HO-1 gene shows length polymorphism and could modul...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/302729

    authors: Yamada N,Yamaya M,Okinaga S,Nakayama K,Sekizawa K,Shibahara S,Sasaki H

    更新日期:2000-01-01 00:00:00

  • Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects.

    abstract::Genetic defects affecting motility of cilia and flagella cause chronic destructive airway disease, randomization of left-right body asymmetry, and, frequently, male infertility in primary ciliary dyskinesia (PCD). The most frequent defects involve outer and inner dynein arms (ODAs and IDAs) that are large multiprotein...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2009.10.018

    authors: Loges NT,Olbrich H,Becker-Heck A,Häffner K,Heer A,Reinhard C,Schmidts M,Kispert A,Zariwala MA,Leigh MW,Knowles MR,Zentgraf H,Seithe H,Nürnberg G,Nürnberg P,Reinhardt R,Omran H

    更新日期:2009-12-01 00:00:00

  • Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia.

    abstract::To resolve the phylogeny of the autochthonous mitochondrial DNA (mtDNA) haplogroups of India and determine the relationship between the Indian and western Eurasian mtDNA pools more precisely, a diverse subset of 75 macrohaplogroup N lineages was chosen for complete sequencing from a collection of >800 control-region s...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1086/425871

    authors: Palanichamy MG,Sun C,Agrawal S,Bandelt HJ,Kong QP,Khan F,Wang CY,Chaudhuri TK,Palla V,Zhang YP

    更新日期:2004-12-01 00:00:00

  • Resequencing candidate genes implicates rare variants in asthma susceptibility.

    abstract::Common variation in over 100 genes has been implicated in the risk of developing asthma, but the contribution of rare variants to asthma susceptibility remains largely unexplored. We selected nine genes that showed the strongest signatures of weak purifying selection from among 53 candidate asthma-associated genes, an...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2012.01.008

    authors: Torgerson DG,Capurso D,Mathias RA,Graves PE,Hernandez RD,Beaty TH,Bleecker ER,Raby BA,Meyers DA,Barnes KC,Weiss ST,Martinez FD,Nicolae DL,Ober C

    更新日期:2012-02-10 00:00:00

  • Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases.

    abstract::Molecular analysis of the human beta-galactosidase gene revealed six different mutations in 10 of 11 Japanese GM1-gangliosidosis patients. They were the only abnormalities in each allele examined in this study. A 165-nucleotide duplication (positions 1103-1267) was found in two infantile patients, producing an abnorma...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Yoshida K,Oshima A,Shimmoto M,Fukuhara Y,Sakuraba H,Yanagisawa N,Suzuki Y

    更新日期:1991-08-01 00:00:00

  • A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects.

    abstract::Richieri-Costa-Pereira syndrome is an autosomal-recessive acrofacial dysostosis characterized by mandibular median cleft associated with other craniofacial anomalies and severe limb defects. Learning and language disabilities are also prevalent. We mapped the mutated gene to a 122 kb region at 17q25.3 through identity...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2013.11.020

    authors: Favaro FP,Alvizi L,Zechi-Ceide RM,Bertola D,Felix TM,de Souza J,Raskin S,Twigg SR,Weiner AM,Armas P,Margarit E,Calcaterra NB,Andersen GR,McGowan SJ,Wilkie AO,Richieri-Costa A,de Almeida ML,Passos-Bueno MR

    更新日期:2014-01-02 00:00:00

  • Refined genetic localization for central core disease.

    abstract::Central core disease (CCO) is an autosomal dominant myopathy clinically distinct from malignant hyperthermia (MHS). In a large kindred in which the gene for CCO is segregating, two-point linkage analysis gave a maximum lod score, between the central core disease locus (CCO) and the ryanodine receptor locus (RYR1), of ...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Mulley JC,Kozman HM,Phillips HA,Gedeon AK,McCure JA,Iles DE,Gregg RG,Hogan K,Couch FJ,MacLennan DH

    更新日期:1993-02-01 00:00:00

  • Canavan disease: mutations among Jewish and non-Jewish patients.

    abstract::Canavan disease is an autosomal recessive leukodystrophy caused by the deficiency of aspartoacylase (ASPA). Sixty-four probands were analyzed for mutations in the ASPA gene. Three point mutations--693C-->A, 854A-->C, and 914C-->A--were identified in the coding sequence. The 693C-->A and 914C-->A base changes, resultin...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Kaul R,Gao GP,Aloya M,Balamurugan K,Petrosky A,Michals K,Matalon R

    更新日期:1994-07-01 00:00:00

  • Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease.

    abstract::Charcot-Marie-Tooth disease is characterized by length-dependent axonal degeneration with distal sensory loss and weakness, deep-tendon-reflex abnormalities, and skeletal deformities. It is caused by mutations in more than 40 genes. We investigated a four-generation family with 23 members affected by the axonal form (...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2011.07.002

    authors: Weedon MN,Hastings R,Caswell R,Xie W,Paszkiewicz K,Antoniadi T,Williams M,King C,Greenhalgh L,Newbury-Ecob R,Ellard S

    更新日期:2011-08-12 00:00:00

  • Association of attention-deficit disorder and the dopamine transporter gene.

    abstract::Attention-deficit hyperactivity disorder (ADHD) has been shown to be familial and heritable, in previous studies. As with most psychiatric disorders, examination of pedigrees has not revealed a consistent Mendelian mode of transmission. The response of ADHD patients to medications that inhibit the dopamine transporter...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Cook EH Jr,Stein MA,Krasowski MD,Cox NJ,Olkon DM,Kieffer JE,Leventhal BL

    更新日期:1995-04-01 00:00:00

  • A linkage study of cystic fibrosis in extended multigenerational pedigrees.

    abstract::The linkage of polymorphic DNA markers on chromosome 7 to cystic fibrosis (CF) was examined in two pedigrees and a number of smaller nuclear families. The pedigrees are multigenerational and together consist of more than 300 members including 30 affected individuals, while the nuclear families each have two generation...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:

    authors: Watkins PC,Schwartz R,Hoffman N,Stanislovitis P,Doherty R,Klinger K

    更新日期:1986-12-01 00:00:00

  • From Peas to Disease: Modifier Genes, Network Resilience, and the Genetics of Health.

    abstract::Phenotypes are rarely consistent across genetic backgrounds and environments, but instead vary in many ways depending on allelic variants, unlinked genes, epigenetic factors, and environmental exposures. In the extreme, individuals carrying the same causal DNA sequence variant but on different backgrounds can be class...

    journal_title:American journal of human genetics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ajhg.2017.06.004

    authors: Riordan JD,Nadeau JH

    更新日期:2017-08-03 00:00:00

  • Smoking, DNA Methylation, and Lung Function: a Mendelian Randomization Analysis to Investigate Causal Pathways.

    abstract::Whether smoking-associated DNA methylation has a causal effect on lung function has not been thoroughly evaluated. We first investigated the causal effects of 474 smoking-associated CpGs on forced expiratory volume in 1 s (FEV1) in UK Biobank (n = 321,047) by using two-sample Mendelian randomization (MR) and then repl...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2020.01.015

    authors: Jamieson E,Korologou-Linden R,Wootton RE,Guyatt AL,Battram T,Burrows K,Gaunt TR,Tobin MD,Munafò M,Davey Smith G,Tilling K,Relton C,Richardson TG,Richmond RC

    更新日期:2020-03-05 00:00:00

  • Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci.

    abstract::Blood pressure (BP) is a heritable risk factor for cardiovascular disease. To investigate genetic associations with systolic BP (SBP), diastolic BP (DBP), mean arterial pressure (MAP), and pulse pressure (PP), we genotyped ~50,000 SNPs in up to 87,736 individuals of European ancestry and combined these in a meta-analy...

    journal_title:American journal of human genetics

    pub_type: 杂志文章,meta分析

    doi:10.1016/j.ajhg.2013.12.016

    authors: Tragante V,Barnes MR,Ganesh SK,Lanktree MB,Guo W,Franceschini N,Smith EN,Johnson T,Holmes MV,Padmanabhan S,Karczewski KJ,Almoguera B,Barnard J,Baumert J,Chang YP,Elbers CC,Farrall M,Fischer ME,Gaunt TR,Gho JM,Gieg

    更新日期:2014-03-06 00:00:00

  • Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement.

    abstract::Cone-rod dystrophy (CRD) and retinitis pigmentosa (RP) are clinically and genetically overlapping heterogeneous retinal dystrophies. By using homozygosity mapping in an individual with autosomal-recessive (ar) RP from a consanguineous family, we identified three sizeable homozygous regions, together encompassing 46 Mb...

    journal_title:American journal of human genetics

    pub_type: 杂志文章

    doi:10.1016/j.ajhg.2011.11.015

    authors: Estrada-Cuzcano A,Neveling K,Kohl S,Banin E,Rotenstreich Y,Sharon D,Falik-Zaccai TC,Hipp S,Roepman R,Wissinger B,Letteboer SJ,Mans DA,Blokland EA,Kwint MP,Gijsen SJ,van Huet RA,Collin RW,Scheffer H,Veltman JA,Zrenne

    更新日期:2012-01-13 00:00:00