14 research outputs found
Scaling and Correlation Functions to Map and Understand the Heterogeneity of the Productive Layer
One of the most challenging problems in the development stage of a field is the prediction of the fluid type as well as lateral and vertical heterogeneities in the reservoir away from the well-location. This multi-scale approach, both downscaling and upscaling to the solution is a two-step process based on the Pair Correlation Function (PCF) approximation method that takes into account the effect of scattering by considering the interactions between any two points of a heterogeneous medium. The amplitude of the correlations of fluctuations are estimated for various combinations of measured and calculated physical properties like velocity, density, porosity, and elastic stiffness tensors. The fluctuations will be higher if the medium is heterogeneous due to sudden changes in lithology or if the properties of the inclusions are drastically different from the matrix, as in the case of a productive layer and so we expect higher values for amplitude.
The first step is to detect the heterogeneous layer from the well-logs for a range of frequencies. Hermite Distributed Approximating Functionals (HDAFs) and Simple Moving Average (SMA) are used as the averaging or upscaling methods for calculating the amplitude of the fluctuations. The results show that to detect the productive layers at lower frequencies that corresponds to seismic data, HDAF gives better results. The second step is downscaling where logs are predicted from the seismic data using scaled functions, which are then used to identify and map the heterogeneous layer and predict future well locations. This methodology is also applied to study the heterogeneity in a meandering fluvial channel fill using well–logs in the clastic Tertiary sediments of northern part of South Marsh Island in the Gulf of Mexico (GoM).Earth and Atmospheric Sciences, Department o
Alignment of Homologous Chromosomes and Effective Repair of Programmed DNA Double-Strand Breaks during Mouse Meiosis Require the Minichromosome Maintenance Domain Containing 2 (MCMDC2) Protein.
Orderly chromosome segregation during the first meiotic division requires meiotic recombination to form crossovers between homologous chromosomes (homologues). Members of the minichromosome maintenance (MCM) helicase family have been implicated in meiotic recombination. In addition, they have roles in initiation of DNA replication, DNA mismatch repair and mitotic DNA double-strand break repair. Here, we addressed the function of MCMDC2, an atypical yet conserved MCM protein, whose function in vertebrates has not been reported. While we did not find an important role for MCMDC2 in mitotically dividing cells, our work revealed that MCMDC2 is essential for fertility in both sexes due to a crucial function in meiotic recombination. Meiotic recombination begins with the introduction of DNA double-strand breaks into the genome. DNA ends at break sites are resected. The resultant 3-prime single-stranded DNA overhangs recruit RAD51 and DMC1 recombinases that promote the invasion of homologous duplex DNAs by the resected DNA ends. Multiple strand invasions on each chromosome promote the alignment of homologous chromosomes, which is a prerequisite for inter-homologue crossover formation during meiosis. We found that although DNA ends at break sites were evidently resected, and they recruited RAD51 and DMC1 recombinases, these recombinases were ineffective in promoting alignment of homologous chromosomes in the absence of MCMDC2. Consequently, RAD51 and DMC1 foci, which are thought to mark early recombination intermediates, were abnormally persistent in Mcmdc2-/- meiocytes. Importantly, the strand invasion stabilizing MSH4 protein, which marks more advanced recombination intermediates, did not efficiently form foci in Mcmdc2-/- meiocytes. Thus, our work suggests that MCMDC2 plays an important role in either the formation, or the stabilization, of DNA strand invasion events that promote homologue alignment and provide the basis for inter-homologue crossover formation during meiotic recombination
Chromosomal synapsis defects can trigger oocyte apoptosis without elevating numbers of persistent DNA breaks above wild-type levels
Generation of haploid gametes depends on a modified version of homologous recombination in meiosis. Meiotic recombination is initiated by single-stranded DNA (ssDNA) ends originating from programmed DNA double-stranded breaks (DSBs) that are generated by the topoisomerase-related SPO11 enzyme. Meiotic recombination involves chromosomal synapsis, which enhances recombination-mediated DSB repair, and thus, crucially contributes to genome maintenance in meiocytes. Synapsis defects induce oocyte apoptosis ostensibly due to unrepaired DSBs that persist in asynaptic chromosomes. In mice, SPO11-deficient oocytes feature asynapsis, apoptosis and, surprisingly, numerous foci of the ssDNA-binding recombinase RAD51, indicative of DSBs of unknown origin. Hence, asynapsis is suggested to trigger apoptosis due to inefficient DSB repair even in mutants that lack programmed DSBs. By directly detecting ssDNAs, we discovered that RAD51 is an unreliable marker for DSBs in oocytes. Further, SPO11-deficient oocytes have fewer persistent ssDNAs than wild-type oocytes. These observations suggest that oocyte quality is safeguarded in mammals by a synapsis surveillance mechanism that can operate without persistent ssDNAs.Deutsche Forschungsgemeinschaft (DFG) [TO421/3-1/2, TO421/5-1, TO421/6-1/2, TO421/7-1, TO421/8-1/2, TO421/10-1, TO421/11-1, TO421/12-1]; HFSP research grant [RGP0008/2015 to K.R., R.R., F.P., A.T.]; Ministry of Science, Innovation and Universities of Spain (MCIU/AEI/FEDER, EU) [RTI2018-099055-B-I00]; ‘Junta de Castilla y León’ of Spain (FEDER, EU) [CSI259P20 to P.A.S.S.]. Funding for open access charge: DFG, SLUB
Preferential expression of <i>Mcmdc2</i> in the gonads, and <i>Mcmdc2</i> targeting in mice.
<p>(<b>a</b>) Expression of <i>Mcmdc2</i> and a “house-keeping” gene (<i>S9</i>) in testis and a somatic tissue mix measured by RT-PCR. cDNAs were prepared from four RNA mixtures: (1) Equal amounts of RNAs from 17 somatic tissues (see <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1006393#sec012" target="_blank">Materials and Methods</a> for the tissue list) were mixed and 1μg of the resulting mixture was used for RT (17 somatic tissues). (2) Mixture “1” supplemented with testis RNA at a concentration equal to that of the individual somatic RNAs (17 somatic tissues + 1x testis). (3) Mixture “1” supplemented with testis RNA at a concentration equal to five times that of the individual somatic RNAs (17 somatic tissues + 5 x testis) (4) Mixture “3” with no RT (17 somatic tissues + 5xtestis noRT). <i>Mcmdc2</i>-specific PCR-products were amplified preferentially from templates that contained testis cDNA. (<b>b</b>) <i>Mcmdc2</i> targeting strategy. Schematics of the targeting construct, the wild-type (WT) and the modified <i>Mcmdc2</i> genomic locus. Black boxes represent exons (not to scale). Recombination at the homology arms (HA) of the targeting construct modifies intron 4 by introducing: 1) an additional exon (SA-IRES-LacZ) that contains a strong splice acceptor site (SA) and poly-adenylation site (left grey box), 2) a transcriptional unit that contains the strong housekeeping human ß-Actin promotor <i>(hBactP)</i> driving the neomycin (Neo) resistance gene as a selection marker. This modification of intron 4 also disrupts the <i>Mcmdc2</i> open reading frame after the 95th codon <i>(Mcmdc2</i><sup><i>insertion</i></sup> allele). Recombination catalyzed by FLPe at FRT sites removes the SA-IRES-LacZ exon and the hBactP-Neo gene, and restores the MCMDC2 ORF (<i>Mcmdc2</i><sup><i>restored</i></sup>). <i>Mcmdc2</i><sup><i>restored</i></sup> is a functional allele that can be disrupted by Cre-mediated recombination between loxP sites (<i>Mcmdc2</i><sup><i>deletion</i></sup>). Excision of exon 5–7 causes a frameshift after the 80th codon. Cre-mediated recombination between loxP sites of a <i>Mcmdc2</i><sup><i>insertion</i></sup> allele results in <i>Mcmdc2</i><sup><i>insertion-deletion</i></sup> allele. The positions of PCR-genotyping primers are indicated. Red bars mark the 3`and the internal Southern blot probes; the predicted length of restriction fragments is indicated. (<b>c</b>) Southern blot of DNA from wild-type (+/+) and targeted <i>Mcmdc2</i><sup><i>+/insertion</i></sup> (<i>+/i</i>) embryonic stem cell clones (C6 and F7) that were used to derive two independent mouse lines. DNA was digested with Eco31I and hybridized with an internal probe for LacZ (left panel), or DNA was digested with BclI and hybridized with a 3’ probe (right panel). The blots indicate a single integration of the targeting cassette in the <i>Mcmdc2</i> locus. (<b>d</b>) RT-PCR was used to detect <i>Mcmdc2</i> and "house-keeping" <i>Rps9 (S9)</i> transcripts in testes of wild-type and <i>Mcmdc2</i><sup><i>-/-</i></sup> (insertion-deletion) mice. Oligo-pairs specific to <i>Mcmdc2</i> exon 3 and 4, 5 and 6, 6 and 7, 8 and 9, or 10 and 11 were used.</p
RAD51 and DMC1 foci persist in <i>Mcmdc2</i><sup><i>-/-</i></sup> <i>s</i>permatocytes.
<p>(<b>a, b, e</b>) Immunostaining showing SYCP3 together with RAD51 (<b>a</b>), DMC1 (<b>b</b>) or γH2AX (<b>e</b>) on nuclear surface spreads of pachytene <i>Mcmdc2</i><sup><i>+/+</i></sup>, late zygotene-pachytene <i>Mcmdc2</i><sup><i>-/-</i></sup>, <i>Spo11</i><sup><i>-/-</i></sup>, and <i>Spo11</i><sup><i>-/-</i></sup> <i>Mcmdc2</i><sup><i>-/—</i></sup>spermatocytes. RAD51 and DMC1 foci are present at comparatively high density along the axes of unsynapsed sex chromosomes (<b>a, b</b>, asterisk), and are largely absent from synapsed autosomes of <i>Mcmdc2</i><sup><i>+/+</i></sup> spermatocytes. Both RAD51 and DMC1 foci are present in high numbers along the unpaired axes of <i>Mcmdc2</i><sup><i>-/-</i></sup> spermatocytes. Absence of RAD51 and DMC1 foci is shown in <i>Spo11</i><sup><i>-/-</i></sup> and <i>Spo11</i><sup><i>-/-</i></sup> <i>Mcmdc2</i><sup><i>-/—</i></sup>spermatocytes. (<b>e</b>) γH2AX preferentially accumulates on the partially synapsed sex chromosomes of the <i>Mcmdc2</i><sup><i>+/+</i></sup> spermatocyte. γH2AX associates with chromatin throughout the nucleus in the <i>Mcmdc2</i><sup><i>-/-</i></sup> spermatocytes. γH2AX is largely restricted to the sex chromatin in wild-type pachytene spermatocytes, and to pseudo-sex bodies in <i>Spo11</i><sup><i>-/-</i></sup> and <i>Spo11</i><sup><i>-/-</i></sup> <i>Mcmdc2</i><sup><i>-/—</i></sup>spermatocytes. Scale bars; 10μm. (<b>c, d</b>) Numbers of RAD51 (<b>c</b>) or DMC1 (<b>d</b>) foci are shown in leptotene (lepto), early zygotene (e zygo) in <i>Mcmdc2</i><sup><i>+/+</i></sup> and <i>Mcmdc2</i><sup><i>-/-</i></sup>, late zygotene (l zygo) and early-mid pachytene (e-m pa) in <i>Mcmdc2</i><sup><i>+/+</i></sup> and zygotene-pachytene (zyg-pa) in <i>Mcmdc2</i><sup><i>-/-</i></sup> spermatocytes. Median numbers of foci are marked, and n corresponds to the number of analyzed spermatocytes in three pooled experiments. DMC1 and RAD51 foci numbers are significantly higher in zygotene-pachytene <i>Mcmdc2</i><sup><i>-/-</i></sup> spermatocytes than in late-zygotene or early-mid-pachytene <i>Mcmdc2</i><sup><i>+/+</i></sup> spermatocytes (Mann Whitney test).</p
MCMDC2 is not required for extensive non-homologous synaptonemal complex formation in the <i>Spo11</i><sup><i>-/-</i></sup> background.
<p>(<b>a</b>) SYCP3 (axis marker) and SYCP1 (synaptonemal complex marker) were detected by immunofluorescence on nuclear surface spreads of zygotene-pachytene <i>Mcmdc2</i><sup><i>-/-</i></sup>, <i>Spo11</i><sup><i>-/-</i></sup> or <i>Spo11</i><sup><i>-/-</i></sup> <i>Mcmdc2</i><sup><i>-/—</i></sup>spermatocytes. Whereas comparatively few synaptonemal complex stretches are detected in the <i>Mcmdc2</i><sup><i>-/-</i></sup>spermatocyte, extensive non-homologous synaptonemal complex formation is seen in the <i>Spo11</i><sup><i>-/-</i></sup> or <i>Spo11</i><sup><i>-/-</i></sup> <i>Mcmdc2</i><sup><i>-/—</i></sup>spermatocytes. Scale bars; 10μm (<b>b</b>) Quantification of SYCP1 stretch numbers in zygotene-pachytene spermatocytes with fully condensed chromosome axes of the indicated genotypes. The numbers of synaptonemal complex stretches is significantly higher in <i>Spo11</i><sup><i>-/-</i></sup> or <i>Spo11</i><sup><i>-/-</i></sup> <i>Mcmdc2</i><sup><i>-/—</i></sup>spermatocytes than in <i>Mcmdc2</i><sup><i>-/-</i></sup> (Mann Whitney test). The numbers of synaptonemal complex stretches are not significantly different in <i>Spo11</i><sup><i>-/-</i></sup> or <i>Spo11</i><sup><i>-/-</i></sup> <i>Mcmdc2</i><sup><i>-/—</i></sup>spermatocytes (p = 0.8639, Mann Whitney test). Median numbers of foci are marked, and n corresponds to the number of analyzed spermatocytes in two (<i>Spo11</i><sup><i>-/-</i></sup> or <i>Spo11</i><sup><i>-/-</i></sup> <i>Mcmdc2</i><sup><i>-/-</i></sup>) or three (<i>Mcmdc2</i><sup><i>-/-</i></sup>) pooled experiments.</p
MutSγ and MutLγ foci formation are defective in <i>Mcmdc2</i><sup><i>-/-</i></sup> meiocytes.
<p>(<b>a, b, e, f</b>) Immunostaining of SYCP3 together with MSH4 (<b>a, b</b>) or MLH1 (<b>e, f</b>) on nuclear surface spreads of pachytene <i>Mcmdc2</i><sup><i>+/+</i></sup> or zygotene-pachytene <i>Mcmdc2</i><sup><i>-/-</i></sup> meiocytes. (<b>a, b</b>) MSH4 foci are readily detected along synapsed axes of pachytene spermatocytes and oocytes (16dpc). MSH4 foci numbers are much lower in <i>Mcmdc2</i><sup><i>-/-</i></sup> meiocytes. (<b>e, f</b>) Typically, a single MLH1 focus is detected along each synapsed axis pair of <i>Mcmdc2</i><sup><i>+/+</i></sup> pachytene spermatocytes and oocytes (from ovaries of newborn mice). MLH1 foci are not present along the unsynapsed axes of <i>Mcmdc2</i><sup><i>-/-</i></sup> meiocytes. Scale bars; 10μm. (<b>c, d</b>) Numbers of MSH4 foci in <i>Mcmdc2</i><sup><i>+/+</i></sup> and <i>Mcmdc2</i><sup><i>-/-</i></sup> spermatocytes and oocytes. (<b>c</b>) Spermatocytes were examined at leptotene (lepto), early zygotene (e zygo) in <i>Mcmdc2</i><sup><i>+/+</i></sup> and <i>Mcmdc2</i><sup><i>-/-</i></sup>, late zygotene (l zygo) and early-mid pachytene (e-m pa) in <i>Mcmdc2</i><sup><i>+/+</i></sup> and zygotene-pachytene (zyg-pa) in <i>Mcmdc2</i><sup><i>-/-</i></sup> mice. MSH4 foci numbers are significantly lower in <i>Mcmdc2</i><sup><i>-/-</i></sup> than in <i>Mcmdc2</i><sup><i>+/+</i></sup> spermatocytes from early-zygotene stage onwards (Mann Whitney test). (<b>d</b>) Oocytes with fully formed axes (late zygotene and early pachytene) were examined from fetal ovaries at the 16dpc developmental time point. MSH4 foci numbers are significantly lower in <i>Mcmdc2</i><sup><i>-/-</i></sup> than in <i>Mcmdc2</i><sup><i>+/+</i></sup> oocytes (Mann Whitney test). (<b>c, d</b>) Median numbers of foci are marked, and n corresponds to the number of analyzed meiocytes in two pooled experiments.</p
RAD51 and DMC1 foci persist in <i>Mcmdc2</i><sup><i>-/-</i></sup> oocytes.
<p>(<b>a, c, e)</b> Immunostaining of SYCP3 along with RAD51 (<b>a</b>), DMC1 (<b>c</b>) or γH2AX (<b>e</b>) on nuclear surface spreads of pachytene <i>Mcmdc2</i><sup><i>+/+</i></sup>, or zygotene-pachytene <i>Mcmdc2</i><sup><i>-/-</i></sup> oocytes. Oocytes were collected from the ovaries of littermate fetuses at 18dpc, which is a time point when most wild-type oocytes are in the late pachytene stage. RAD51 and DMC1 foci are largely absent from synapsed chromosomes in <i>Mcmdc2</i><sup><i>+/+</i></sup> oocytes. Both RAD51 and DMC1 foci are present in high numbers along the unpaired axes of <i>Mcmdc2</i><sup><i>-/-</i></sup> oocytes. (<b>e</b>) γH2AX is largely absent from the synapsed chromosomes of the <i>Mcmdc2</i><sup><i>+/+</i></sup> oocyte. γH2AX associates with chromatin throughout the nucleus in the <i>Mcmdc2</i><sup><i>-/-</i></sup> oocyte. Scale bars; 10μm. (<b>b, d</b>) Numbers of RAD51 (<b>b</b>) or DMC1 (<b>d</b>) foci are shown in <i>Mcmdc2</i><sup><i>+/+</i></sup> and <i>Mcmdc2</i><sup><i>-/-</i></sup> oocytes at 18dpc. Median numbers of foci are marked, and n corresponds to the number of analyzed oocytes in two pooled experiments. DMC1 and RAD51 foci numbers are significantly higher in <i>Mcmdc2</i><sup><i>-/-</i></sup> than in <i>Mcmdc2</i><sup><i>+/+</i></sup> oocytes (Mann Whitney test).</p
<i>Mcmdc2</i><sup><i>-/-</i></sup> mice are deficient in germ cells from late meiotic prophase onwards in both sexes.
<p>(<b>a, b</b>) Growth curves of five (<b>a</b>) or three (<b>b</b>) independent lines of <i>Mcmdc2</i><sup><i>+/</i>+</sup> (+/+) and <i>Mcmdc2</i><sup><i>-/-</i></sup> mouse embryonic fibroblasts. Cells were grown either without aphidicolin treatment (<b>a</b>) or with aphidicolin treatment for the first 24 hours (<b>b</b>), where 1μM aphidicolin was added at day 0. (<b>a, b</b>) Cell numbers were determined at the indicated time points in three technical replicates of each fibroblast line. Means and standard deviations of the medians of technical triplicates are shown. Growth curves of <i>Mcmdc2</i><sup><i>+/</i>+</sup> and <i>Mcmdc2</i><sup><i>-/-</i></sup> mouse embryonic fibroblasts are not significantly different (<b>a</b>: p = 0.8201, <b>b</b>: p = 0.9932, two-way ANOVA test). (<b>c</b>) Images of <i>Mcmdc2</i><sup><i>+/</i>+</sup> (+/+) and <i>Mcmdc2</i><sup><i>-/-</i></sup> (-/-) testes (upper panel) and ovaries (lower panel). Scale bars; 500μm. (<b>d</b>) Cryosections of testes from adult <i>Mcmdc2</i><sup><i>+/+</i></sup> and <i>Mcmdc2</i><sup><i>-/-</i></sup> mice. DNA was detected by DAPI, histone H1T (marker of spermatocytes after mid-pachytene) and nuclear cleaved PARP1 (marker of apoptotic cells) were detected by immunostaining. Outlines of testis tubules are marked by dashed lines. The upper panels of <b>d</b> show stage V-VI and VII-VIII wild-type testis tubules, which contain several layers of germ cells at distinct spermatogenic stages: Sertoli cells (Se), spermatogonia B (SgB, stage V-VI), preleptotene (pl, stage VII-VIII), mid-pachytene (pa, stage V-VI), late-pachytene (pa, stage VII-VIII) spermatocytes, post-meiotic spermatids (sd) and spermatozoa (sp). Lower panels of <b>d</b> show that <i>Mcmdc2</i><sup><i>-/-</i></sup> meiocytes underwent apoptosis at a stage corresponding to wild-type mid-pachytene in stage IV tubules. Consequently, spermatocytes were not found in the inner layers of testis tubules beyond stage IV, and post-meiotic spermatids and spermatozoa were also missing from <i>Mcmdc2</i><sup><i>-/-</i></sup> testes. To illustrate this, stage IV, V-VI and VII-VIII tubules of <i>Mcmdc2</i><sup><i>-/-</i></sup> mice are shown. Apoptotic (ap) and non-apoptotic early-mid pachytene (pa) spermatocytes are shown in the stage IV tubule, which was identified by the presence of mitotic intermediate spermatogonia (m) and intermediate spermatogonia (Int). Stage V-VI and VII-VIII tubules contain somatic Sertoli cells (Se) and spermatogonia B (SgB) or preleptotene (pl) spermatocytes, respectively, but more advanced spermatogenic cells are missing. Due to elimination at mid-pachytene, histone H1T positive cells are missing from <i>Mcmdc2</i><sup><i>-/-</i></sup> testis tubules. (<b>e</b>) NOBOX (oocyte marker) was detected by immunofluorescence on cryosections of ovaries from 6-week-old mice. DNA was stained by DAPI. Oocytes in primordial (pd) and secondary (s) follicles are shown in the section of a wild-type ovary. In contrast, oocytes are not detected in the shown <i>Mcmdc2</i><sup><i>-/-</i></sup> ovary section. (<b>d, e</b>) Scale bars; 50μm.</p
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Novobiocin blocks nucleic acid binding to Polθ and inhibits stimulation of its ATPase activity.
Polymerase theta (Polθ) acts in DNA replication and repair, and its inhibition is synthetic lethal in BRCA1 and BRCA2-deficient tumor cells. Novobiocin (NVB) is a first-in-class inhibitor of the Polθ ATPase activity, and it is currently being tested in clinical trials as an anti-cancer drug. Here, we investigated the molecular mechanism of NVB-mediated Polθ inhibition. Using hydrogen deuterium exchange-mass spectrometry (HX-MS), biophysical, biochemical, computational and cellular assays, we found NVB is a non-competitive inhibitor of ATP hydrolysis. NVB sugar group deletion resulted in decreased potency and reduced HX-MS interactions, supporting a specific NVB binding orientation. Collective results revealed that NVB binds to an allosteric site to block DNA binding, both in vitro and in cells. Comparisons of The Cancer Genome Atlas (TCGA) tumors and matched controls implied that POLQ upregulation in tumors stems from its role in replication stress responses to increased cell proliferation: this can now be tested in fifteen tumor types by NVB blocking ssDNA-stimulation of ATPase activity, required for Polθ function at replication forks and DNA damage sites. Structural and functional insights provided in this study suggest a path for developing NVB derivatives with improved potency for Polθ inhibition by targeting ssDNA binding with entropically constrained small molecules