The centenary of Janssens's chiasmatype theory.

Abstract:

:The segregation and random assortment of characters observed by Mendel have their basis in the behavior of chromosomes in meiosis. But showing this actually to be the case requires a correct understanding of the meiotic behavior of chromosomes. This was achieved only gradually, over several decades, with much dispute and confusion along the way. One crucial step in the understanding of meiosis was provided in 1909 by Frans Alfons Janssens who published in La Cellule an article entitled "La théorie de la Chiasmatypie. Nouvelle interprétation des cinèses de maturation," which contains the first description of the chiasma structure. He observed that, of the four chromatids present at the connection sites (chiasmata sites) at diplotene or anaphase of the first meiotic division, two crossed each other and two did not. He therefore postulated that the maternal and paternal chromatids that crossed penetrated the other until they broke and rejoined in maternal and paternal segments new ways; the other two chromatids remained free and thus intact. This allowed him also to propose that the chromatids distributed in the four nuclei issued from the second meiotic division had various combinations of maternal and paternal segments of each chromosome. And conversely, permitted the appreciation that the laws of Mendelian segregation required breakage and joining (crossing over) between homologous non-sister chromatids. Although Janssens's article found a broad appreciative audience and had a large influence on the chromosomal theory at that time, his theory was resisted by both geneticists and cytologists for several decades. This Perspectives aims to highlight the novelty of Janssens's chiasmatype theory by examining the historical background and our actual understanding of meiotic recombination.

journal_name

Genetics

journal_title

Genetics

authors

Koszul R,Meselson M,Van Doninck K,Vandenhaute J,Zickler D

doi

10.1534/genetics.112.139733

subject

Has Abstract

pub_date

2012-06-01 00:00:00

pages

309-17

issue

2

eissn

0016-6731

issn

1943-2631

pii

191/2/309

journal_volume

191

pub_type

传,历史文章,杂志文章

相关文献

GENETICS文献大全
  • Amino acid replacements resulting from suppression and missense reversion of a chain-terminator mutation in Neurospora.

    abstract::The Neurospora crassa super-suppressor mutation, ssu-1, suppresses the auxotrophic phenotype of the mutant am(17) by inserting tyrosine at residue 313 of NADP-specific glutamate dehydrogenase, a position occupied in the wild type by glutamate. Two classes of am(17) revertants due to further mutation within the am gene...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Seale TW,Brett M,Baron AJ,Fincham JR

    更新日期:1977-06-01 00:00:00

  • A novel Markov chain monte carlo approach for constructing accurate meiotic maps.

    abstract::Mapping markers from linkage data continues to be a task performed in many genetic epidemiological studies. Data collected in a study may be used to refine published map estimates and a study may use markers that do not appear in any published map. Furthermore, inaccuracies in meiotic maps can seriously bias linkage f...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.042705

    authors: George AW

    更新日期:2005-10-01 00:00:00

  • A genome-wide departure from the standard neutral model in natural populations of Drosophila.

    abstract::We analyze nucleotide polymorphism data for a large number of loci in areas of normal to high recombination in Drosophila melanogaster and D. simulans (24 and 16 loci, respectively). We find a genome-wide, systematic departure from the neutral expectation for a panmictic population at equilibrium in natural population...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Andolfatto P,Przeworski M

    更新日期:2000-09-01 00:00:00

  • Mettl3 Mutation Disrupts Gamete Maturation and Reduces Fertility in Zebrafish.

    abstract::N6-methyladenosine (m6A), catalyzed by Mettl3 methyltransferase, is a highly conserved epigenetic modification in eukaryotic messenger RNA (mRNA). Previous studies have implicated m6A modification in multiple biological processes, but the in vivo function of m6A has been difficult to study, because mettl3 mutants are ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.117.300574

    authors: Xia H,Zhong C,Wu X,Chen J,Tao B,Xia X,Shi M,Zhu Z,Trudeau VL,Hu W

    更新日期:2018-02-01 00:00:00

  • Exegeses on maximum genetic differentiation.

    abstract::A canon of population genetics concerns the properties of FST, a descriptor of spatial genetic structure. Interest for FST arose from Wright's early insights linking FST to dispersal parameters as well as to his concept of effective population size (e.g., Wright 1938, 1951). Although there is continued interest in thi...

    journal_title:Genetics

    pub_type: 评论,杂志文章

    doi:10.1534/genetics.113.152132

    authors: Rousset F

    更新日期:2013-07-01 00:00:00

  • Repair of a mismatch is influenced by the base composition of the surrounding nucleotide sequence.

    abstract::Heteroduplexes with single base pair mismatches of known sequence were prepared by annealing separated strands of bacteriophage lambda DNA and used to transfect Escherichia coli. A series of transition (G:T and A:C) and transversion (G:A and C:T) mismatches located throughout most of the bacteriophage lambda cI gene h...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Jones M,Wagner R,Radman M

    更新日期:1987-04-01 00:00:00

  • Repeated Duplication of Argonaute2 Is Associated with Strong Selection and Testis Specialization in Drosophila.

    abstract::Argonaute2 (Ago2) is a rapidly evolving nuclease in the Drosophila melanogaster RNA interference (RNAi) pathway that targets viruses and transposable elements in somatic tissues. Here we reconstruct the history of Ago2 duplications across the D. obscura group and use patterns of gene expression to infer new functional...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.116.192336

    authors: Lewis SH,Webster CL,Salmela H,Obbard DJ

    更新日期:2016-10-01 00:00:00

  • A screen for mutations that suppress the phenotype of Drosophila armadillo, the beta-catenin homolog.

    abstract::During development signaling pathways coordinate cell fates and regulate the choice between cell survival or programmed cell death. The well-conserved Wingless/Wnt pathway is required for many developmental decisions in all animals. One transducer of the Wingless/Wnt signal is Armadillo/beta-catenin. Drosophila Armadi...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Cox RT,McEwen DG,Myster DL,Duronio RJ,Loureiro J,Peifer M

    更新日期:2000-08-01 00:00:00

  • On the interpretation of mutagenically induced mosaicism in Drosophila.

    abstract::This paper draws attention to the formal parallelism that exists between chromosomal-loss mosaicism and mutagenically induced mosaicism in Drosophila and suggests that, although the underlying processes by which these two types of genetic mosaics are generated are very different, the more refined methodology employed ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Nissani M

    更新日期:1977-08-01 00:00:00

  • Efficient Genome Editing in Caenorhabditis elegans with a Toolkit of Dual-Marker Selection Cassettes.

    abstract::Use of the CRISPR/Cas9 RNA-guided endonuclease complex has recently enabled the generation of double-strand breaks virtually anywhere in the C. elegans genome. Here, we present an improved strategy that makes all steps in the genome editing process more efficient. We have created a toolkit of template-mediated repair ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.180679

    authors: Norris AD,Kim HM,Colaiácovo MP,Calarco JA

    更新日期:2015-10-01 00:00:00

  • The genetic structure of a tribal population, the Yanomama Indians. XIV. Clines and their interpretation.

    abstract::The Yanomama Indians are a South American tribe distributed over an irregular area approximately 200 X 300 miles. The gene frequencies observed at 12 loci in 47 villages within this area have been analyzed for the occurrence of clines. Apparently significant clines are observed for alleles of the Rh, MNSs, Kidd, Gm, I...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Ward RH,Neel JV

    更新日期:1976-01-01 00:00:00

  • Extended Synaptotagmin Localizes to Presynaptic ER and Promotes Neurotransmission and Synaptic Growth in Drosophila.

    abstract::The endoplasmic reticulum (ER) is an extensive organelle in neurons with important roles at synapses including the regulation of cytosolic Ca2+, neurotransmission, lipid metabolism, and membrane trafficking. Despite intriguing evidence for these crucial functions, how the presynaptic ER influences synaptic physiology ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.117.300261

    authors: Kikuma K,Li X,Kim D,Sutter D,Dickman DK

    更新日期:2017-11-01 00:00:00

  • Hardy-Weinberg testing of a single homozygous genotype.

    abstract::No proper statistical test is available for the evaluation of deviation of a single homozygous genotype from Hardy-Weinberg equilibrium (HWE) proportion. We propose a 1-d.f. chi2-test. The power of the proposed test is favorable compared to existing HWE testing procedures. The applications of this test are discussed. ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.043190

    authors: Chen JJ,Duan T,Single R,Mather K,Thomson G

    更新日期:2005-07-01 00:00:00

  • No Cost of Complexity in Bacteriophages Adapting to a Complex Environment.

    abstract::A long-standing prediction in evolutionary biology is that organisms experience a so-called "cost of complexity" manifested as a decreasing rate of adaptation in populations as organisms or selective environments become increasingly complex. This theory assumes the ubiquity of antagonistic pleiotropy, or trade-offs in...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.119.302029

    authors: Sackman AM,Rokyta DR

    更新日期:2019-05-01 00:00:00

  • Genetic Architectures of Quantitative Variation in RNA Editing Pathways.

    abstract::RNA editing refers to post-transcriptional processes that alter the base sequence of RNA. Recently, hundreds of new RNA editing targets have been reported. However, the mechanisms that determine the specificity and degree of editing are not well understood. We examined quantitative variation of site-specific editing i...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.179481

    authors: Gu T,Gatti DM,Srivastava A,Snyder EM,Raghupathy N,Simecek P,Svenson KL,Dotu I,Chuang JH,Keller MP,Attie AD,Braun RE,Churchill GA

    更新日期:2016-02-01 00:00:00

  • Evolution of resistance in the presence of two insecticides.

    abstract::A two-locus model is used to analyze the effectiveness of a mixture of insecticides in delaying resistance, compared to the use of the insecticides singly. The effects of factors such as recombination, effective dominance, initial value of allele frequencies and initial value of linkage disequilibrium are considered. ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Mani GS

    更新日期:1985-04-01 00:00:00

  • Essential, overlapping and redundant roles of the Drosophila protein phosphatase 1 alpha and 1 beta genes.

    abstract::Protein serine/threonine phosphatase type 1 (PP1) has been found in all eukaryotes examined to date and is involved in the regulation of many cellular functions, including glycogen metabolism, muscle contraction, and mitosis. In Drosophila, four genes code for the catalytic subunit of PP1 (PP1c), three of which belong...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.069914

    authors: Kirchner J,Gross S,Bennett D,Alphey L

    更新日期:2007-05-01 00:00:00

  • Recombination can partially substitute for SPO13 in regulating meiosis I in budding yeast.

    abstract::Recombination and chromosome synapsis bring homologous chromosomes together, creating chiasmata that ensure accurate disjunction during reductional division. SPO13 is a key gene required for meiosis I (MI) reductional segregation, but dispensable for recombination, in Saccharomyces cerevisiae. Absence of SPO13 leads t...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Rutkowski LH,Esposito RE

    更新日期:2000-08-01 00:00:00

  • Analysis of quantitative trait loci for behavioral laterality in mice.

    abstract::Laterality is believed to have genetic components, as has been deduced from family studies in humans and responses to artificial selection in mice, but these genetic components are unknown and the underlying physiological mechanisms are still a subject of dispute. We measured direction of laterality (preferential use ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Roubertoux PL,Le Roy I,Tordjman S,Cherfou A,Migliore-Samour D

    更新日期:2003-03-01 00:00:00

  • Structure, expression and phylogenetic analysis of the gene encoding actin I in Pneumocystis carinii.

    abstract::Actin is a major component of the cytoskeleton and one of the most abundant proteins found in eukaryotic cells. Comparative sequence analysis shows that this essential gene has been highly conserved throughout eukaryotic evolution making it useful for phylogenetic analysis. Complete cDNA clones for the actin-encoding ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Fletcher LD,McDowell JM,Tidwell RR,Meagher RB,Dykstra CC

    更新日期:1994-07-01 00:00:00

  • Estimation of deleterious genomic mutation parameters in natural populations by accounting for variable mutation effects across loci.

    abstract::The genomes of all organisms are subject to continuous bombardment of deleterious genomic mutations (DGM). Our ability to accurately estimate various parameters of DGM has profound significance in population and evolutionary genetics. The Deng-Lynch method can estimate the parameters of DGM in natural selfing and outc...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Deng HW,Gao G,Li JL

    更新日期:2002-11-01 00:00:00

  • Repeated Selection of Alternatively Adapted Haplotypes Creates Sweeping Genomic Remodeling in Stickleback.

    abstract::Heterogeneous genetic divergence can accumulate across the genome when populations adapt to different habitats while still exchanging alleles. How long does diversification take and how much of the genome is affected? When divergence occurs in parallel from standing genetic variation, how often are the same haplotypes...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.117.300610

    authors: Bassham S,Catchen J,Lescak E,von Hippel FA,Cresko WA

    更新日期:2018-07-01 00:00:00

  • Genetics of arginine biosynthesis in Neurospora crassa.

    abstract::A large number of arginine-requiring mutants of Neurospora was isolated, using a strain already partially impaired in an enzyme of the pathway. Among the mutants, all previously described loci, except one, were represented, and several new loci were defined and mapped. Four groups of mutants were of particular interes...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Davis RH

    更新日期:1979-11-01 00:00:00

  • Analysis of the multiple roles of gld-1 in germline development: interactions with the sex determination cascade and the glp-1 signaling pathway.

    abstract::The Caenorhabditis elegans gene gld-1 is essential for oocyte development; in gld-1 (null) hermaphrodites, a tumor forms where oogenesis would normally occur. We use genetic epistasis analysis to demonstrate that tumor formation is dependent on the sexual fate of the germline. When the germline sex determination pathw...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Francis R,Maine E,Schedl T

    更新日期:1995-02-01 00:00:00

  • Identification of an alternative oxidase induction motif in the promoter region of the aod-1 gene in Neurospora crassa.

    abstract::The nuclear aod-1 gene of Neurospora crassa encodes the alternative oxidase and is induced when the standard cytochrome-mediated respiratory chain of mitochondria is inhibited. To study elements of the pathway responsible for alternative oxidase induction, we generated a series of mutations in the region upstream from...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.068635

    authors: Chae MS,Lin CC,Kessler KE,Nargang CE,Tanton LL,Hahn LB,Nargang FE

    更新日期:2007-04-01 00:00:00

  • Heterosis as an explanation for large amounts of genic polymorphism.

    abstract::By using both numerical and analytical approaches, we have shown that heterosis alone is not a mechanism for maintaining many alleles segregating at a locus. Even when all heterozygous are more fit than all homozygotes, the proportion of fitness arrays that will lead to a stable, feasible equilibrium of more than 6 or...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Lewontin RC,Ginzburg LR,Tuljapurkar SD

    更新日期:1978-01-01 00:00:00

  • Eukaryotic beta-alanine synthases are functionally related but have a high degree of structural diversity.

    abstract::beta-Alanine synthase (EC 3.5.1.6), which catalyzes the final step of pyrimidine catabolism, has only been characterized in mammals. A Saccharomyces kluyveri pyd3 mutant that is unable to grow on N-carbamyl-beta-alanine as the sole nitrogen source and exhibits diminished beta-alanine synthase activity was used to clon...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Gojković Z,Sandrini MP,Piskur J

    更新日期:2001-07-01 00:00:00

  • Analysis of conditional mutations in the Saccharomyces cerevisiae MLH1 gene in mismatch repair and in meiotic crossing over.

    abstract::In mismatch repair (MMR), members of the MLH gene family have been proposed to act as key molecular matchmakers to coordinate mismatch recognition with downstream repair functions that result in mispair excision. Two members of this gene family, MLH1 and MLH3, have also been implicated in meiotic crossing over. These ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Argueso JL,Smith D,Yi J,Waase M,Sarin S,Alani E

    更新日期:2002-03-01 00:00:00

  • A Bayesian Approach to Inferring Rates of Selfing and Locus-Specific Mutation.

    abstract::We present a Bayesian method for characterizing the mating system of populations reproducing through a mixture of self-fertilization and random outcrossing. Our method uses patterns of genetic variation across the genome as a basis for inference about reproduction under pure hermaphroditism, gynodioecy, and a model de...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.179093

    authors: Redelings BD,Kumagai S,Tatarenkov A,Wang L,Sakai AK,Weller SG,Culley TM,Avise JC,Uyenoyama MK

    更新日期:2015-11-01 00:00:00

  • A genetic screen for dominant modifiers of a small-wing phenotype in Drosophila melanogaster identifies proteins involved in splicing and translation.

    abstract::Studies in the fly, Drosophila melanogaster, have revealed that several signaling pathways are important for the regulation of growth. Among these, the insulin receptor/phosphoinositide 3-kinase (PI3K) pathway is remarkable in that it affects growth and final size without disturbing pattern formation. We have used a s...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.045021

    authors: Coelho CM,Kolevski B,Walker CD,Lavagi I,Shaw T,Ebert A,Leevers SJ,Marygold SJ

    更新日期:2005-10-01 00:00:00