共查询到20条相似文献,搜索用时 15 毫秒
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Klaus Hägele 《Chromosoma》1979,71(2):217-225
The DNA of fixed mitotic and meiotic chromosomes and of spermatides of Schistocerca gregaria males was heat denaturated and then differentially reassociated in a Giemsa buffer or in acridine orange buffer solution. After this procedure, two to three large, selectively stained regions are seen in the X chromosome of spermatocytes and spermatides. Denaturation and reassociation experiments have shown that after differential reassociation such a selective stainability of chromosome regions is characteristic for the presence of fast-reassociating, i.e., repetitive DNA (Stockert and Lisanti, 1972). The possible presence of repetitive DNA in the X chromosome regions concerned can not be the only reason for the occurrence of the heavily stained segments after reassociation because (1) these segments are obtained in positively heteropycnotic X chromosomes, but not in negatively heteropycnotic Xs and (2) they do not occur in positively heteropycnotic X chromosomes when the histones have been extracted before the denaturation and reassociation processes. Contrary to the latter statement, the heavily stained X chromosomal regions are preserved when the histones are removed after the denaturation and reassociation steps. — It is assumed that the heavily stained X chromosome segments represent DNA reassociation complexes which are only formed if histones are present. It is discussed whether the formation of the X chromosome complexes depends on a specific chromatin configuration within positively heteropycnotic X chromosomes. 相似文献
3.
Kathleen Church 《Chromosoma》1979,71(3):359-370
The X chromosome can be identified with the light microscope throughout all stages of the gonial cell cycle (including interphase) in the grasshopper Brachystola magna. At gonial mitotic stages the X chromosome gives the appearance of being undercondensed or negatively heteropycnotic. At interphase the X projects out from the body of the nucleus. — Examination with the electron microscope reveals that the X is compartmentalized at least two gonial cell cycles prior to the entry of the cells into meiotic prophase. The membrane layers that envelope the X chromatin at interphase remain associated with the X chromosome throughout gonial mitotic stages providing the ultrastructural basis for the apparent negative heteropycnosis observed with the light microscope. — The X chromosome is inactive in RNA synthesis during gonial mitotic stages but is hyperactive in RNA synthesis when compared to autosomes at gonial interphase. — X chromosome condensation which reaches its maximum at premieotic interphase is initiated at or prior to the pre-pentultimate gonial division. 相似文献
4.
We have analyzed the anomalous pycnotic cycle of the X sex chromosome of the grasshopper Pyrgomorpha conica throughout both meiotic divisions and its possible influence on spermiogenesis. During diplotene the sex chromosome shows two differentiated pycnotic regions: (i) the centromeric region, which is negatively heteropycnotic, and (ii) the noncentromeric region, which shows alternating negatively and positively heteropycnotic zones in all standard individuals. The variation in size and location of the negative heteropycnotic zones, their smooth appearance, and their lack of effect on spermiogenesis lead us to suggest that condensation differences and not euchromatinization are responsible for their presence. In two individuals the sex chromosome appeared partially isopycnotic at metaphase I, and high levels of abnormal spermatids (macrospermatids and microspermatids) were found. We suggest that the possible activity of this chromosome during the second meiotic division may promote the disruption of spermiogenesis by affecting the mechanism that maintains intercellular bridges between normal spermatids. 相似文献
5.
Uzi Nur 《Chromosoma》1978,68(2):165-185
In short-horned grasshoppers the X chromosome is negatively heteropycnotic in at least some of the spermatogonia but is positively heteropycnotic (heterochromatic) during prophase I of spermatogenesis. In tetraploid (4n) spermatocytes in prophase I the two Xs present have so far been reported always to be heterochromatic and unpaired. In several males of the grasshopper Melanoplus femur-rubrum (Acrididae), however, some of the 4n primary spermatocytes contained one heterochromatic X (Xh) and one euchromatic X (Xe). This asymmetry of heteropycnosis (AH) was first observed in grasshoppers by M.J.D. White who observed it, however, only in 4n spermatogonia in which one X was negatively heteropycnotic and the other was isopycnotic (euchromatic). In M. femur-rubrum the AH involved both positive and negative heteropycnosis. In some of the 4n cells both Xs were heterochromatic and these cells were usually present in small groups but sometimes comprised whole cysts. The 4n cells with Xe+Xh always comprised several whole cysts in a follicle or whole follicles. The origin of the two cell types may be explained by assuming that heteropycnosis originated prior to the origin of the cysts, that when, as a result of polyploidization, two Xs were present in a 4n cell only one became heteropycnotic, and that the state of the X (Xh vs. Xe) usually persisted into meiosis. The 4n primary spermatocytes exhibiting AH divided regularly during the first meiotic division but following telophase I they usually failed to undergo cytokinesis and to enter the second meiotic division. The available evidence suggests that the arrest of these cells is the result of the genetic activity of the Xe in those stages in which the X is usually heterochromatic and genetically inactive. The relationship between AH and facultative heterochromatinization is discussed and it is concluded that the present observations put into question the validity of previous models attempting to explain facultative heterochromatinization (including that of the X in the mammalian female). 相似文献
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The australian plague locust (2n=23 male, 24 female) is distinctive in possessing three pairs of two-armed, short autosomes (S9, S10 and S11). In two of these pairs (S9, S10) these arms are a constant feature but in the shortest (S9) pair most individuals are either heterozygous for them or else are homozygous telocentric. Coupled with this five of the heterozygous individuals give evidence of occasional short-arm detachment.—In all the S-pairs the shorter of the two arms is invariably heterochromatic in character and in the S9 and S11 shows a bi- or tri-partite sub-structure which suggests they may have originated by tandem duplication. — Three of the other autosomes (L2, M3 and M6) also have small heterochromatin(het)-blocks associated with them. At first meiotic prophase these frequently associate with the univalent X chromosome which itself displays an unconventional pattern of allocycly, its centric end appearing negatively heteropycnotic from leptotene through diplotene.—At metaphase I the het-blocks on the telocentric autosomes sometimes transform into swollen, negatively heteropycnotic, segments equivalent in appearance to that shown by the entire X at this stage. It is suggested that these puff-like structures represent an inter-chromosomal position effect conditional upon prior X/A het-association at first prophase. 相似文献
8.
M. J. D. White 《Chromosoma》1970,30(1):51-61
In XO male grasshoppers (Acridoidea and Eumastacoidea) X-chromatin is negatively heteropycnotic in spermatogonial mitoses. In neo-XY species which have a fusion between the original X and an autosome it is usual for the former alone to show negative heteropycnosis. This is the case in the Australian Morabine grasshopper species P52a. In tetraploid spermatogonia of this species, however, which contain two neo-X's and two neo-Y's, only one of the neo-X's has a negatively heteropycnotic left limb, the other X having the same degree of condensation as the autosomes. This novel type of behavior is compared with the heteropycnosis of one of the two X's in the somatic cells of female mammals. It is concluded that the asymmetry of condensation of the two X's in tetraploid spermatogonia of P52a demonstrates the existence of a fundamental cellular mechanism which is inherent and only expressed under the abnormal condition of tetraploidy.Supported by Public Health Service Grant GM-07212 from the Division of General Medical Sciences, U.S. National Institutes of Health and by a grant from the Australian Research Grants Committee. 相似文献
9.
Joanne L. Thorvaldsen Christopher Krapp Huntington F. Willard Marisa S. Bartolomei 《Genetics》2012,192(3):1095-1107
During the development of female mammals, one of the two X chromosomes is inactivated, serving as a dosage-compensation mechanism to equalize the expression of X-linked genes in females and males. While the choice of which X chromosome to inactivate is normally random, X chromosome inactivation can be skewed in F1 hybrid mice, as determined by alleles at the X chromosome controlling element (Xce), a locus defined genetically by Cattanach over 40 years ago. Four Xce alleles have been defined in inbred mice in order of the tendency of the X chromosome to remain active: Xcea < Xceb < Xcec < Xced. While the identity of the Xce locus remains unknown, previous efforts to map sequences responsible for the Xce effect in hybrid mice have localized the Xce to candidate regions that overlap the X chromosome inactivation center (Xic), which includes the Xist and Tsix genes. Here, we have intercrossed 129S1/SvImJ, which carries the Xcea allele, and Mus musculus castaneus EiJ, which carries the Xcec allele, to generate recombinant lines with single or double recombinant breakpoints near or within the Xce candidate region. In female progeny of 129S1/SvImJ females mated to recombinant males, we have measured the X chromosome inactivation ratio using allele-specific expression assays of genes on the X chromosome. We have identified regions, both proximal and distal to Xist/Tsix, that contribute to the choice of which X chromosome to inactivate, indicating that multiple elements on the X chromosome contribute to the Xce. 相似文献
10.
《Journal of bryology》2013,35(3):422-426
Abstract1. In six species of hepatics belonging to the Marchantiales and Acrogynae the large heteropycnotic chromosome found in addition to the sex chromosome or microchromosome is the nucleolar chromosome.2. The sex chromosomes and microchromosomes in these species, and in four of the five species of which the nucleolar chromosomes have been described by other authors, are not nucleolar chromosomes. Riccardia pinguis (L.) Gray appears to stand alone in having a nucleolar orpnizer on the sex chromosome in addition to that on an autosome bearing a heteropycnotic trabant.3. The large heteropycnotic sex chromosomes of certain species of Frullania belonging to the subgenus Galeiloba Steph. are not apparently homologous with the large heteropycnotic chromosome of Frullania africana Steph., belonging to the subgenus Chonanthelia Spr. This is not in accordance with the suggestion of Tatuno (1941) that all ' H-chromosomes' are phylogenetically homologous.4. It is argued that the nucleolar chromosomes throughout the hepatics, with the exception of the sex chromosome of Riccardia pinguis, may be phylogenetically homologous. 相似文献
11.
In spite of various cytogenetic works on suborder Heteroptera, the chromosome organization, function and its evolution in this group is far from being fully understood. Cytologically, the family Rhyparochromidae constitutes a heterogeneous group differing in chromosome numbers. This family possesses XY sex mechanism in the majority of the species with few exceptions. In the present work, multiple banding techniques viz., C-banding, base-specific fluorochromes (DAPI/CMA3) and silver nitrate staining have been used to cytologically characterize the chromosomes of the seed plant pest Elasmolomus (Aphanus) sordidus Fabricius, 1787 having 2n=12=8A+2m+XY. One pair of the autosomes was large while three others were of almost equal size. At diplotene, C-banding technique revealed, that three autosomal bivalents show terminal constitutive heterochromatic bands while one medium sized bivalent was euchromatic. Microchromosomes (m-chromosomes) were positively heteropycnotic. After DAPI and CMA3 staining, all the autosomal bivalents showed equal fluorescence, except CMA3 positive signals, observed at both telomeric heterochromatic regions of one medium sized autosomal bivalent. Silver nitrate staining further revealed that this chromosome pair carries Nucleolar Organizer Regions (NORs) at the location of CMA3 positive signals. The X chromosome showed a thick C-band, positive to both DAPI /CMA3 while Y, otherwise C-negative, was weakly positive to DAPI and negative to CMA3, m-chromosomes were DAPI bright and CMA3 dull. 相似文献
12.
Jun-ichi Suto 《Mammalian genome》2011,22(11-12):648-660
In the present study, dissection of genetic bases of testis weight in mice was performed. Autosomes and the X chromosome were searched using traditional quantitative trait locus (QTL) scans, and the Y chromosome was searched by association studies of Y-consomic strains. QTL analysis was performed in ??DDD?×???CBA F2 mice; the inbred mouse DDD has the heaviest testes, whereas the inbred mouse CBA has the lightest testes. Two significant testis weight QTLs were identified on chromosomes 1 and X. A DDD allele was associated with increased and decreased testis weight at the locus on chromosomes 1 and X, respectively. In the reciprocal cross ??CBA?×???DDD F2 mice, QTL on chromosome 1, and not on chromosome X, had a significant effect on testis weight. The DDD allele at the X-linked locus could not sustain testis weight in combination with the Y chromosome of the CBA strain. The Y chromosome per se had a significant effect on testis weight, i.e., DH-Chr YDDD had significantly heavier testes than DH-Chr YCBA. On the basis of the results of Y-chromosome-wide association studies using 17 Y-consomic strains, variations in Uty, Usp9y, and Sry were significantly associated with testis weight. Thus, testis weight is a complex quantitative phenotype controlled by multiple genes on autosomes and sex chromosomes and their interactions. 相似文献
13.
Polysomes have been prepared from Acheta male accessory gland. The following factors are important in ensuring maximum yield: (1) homogenization at a large buffer to tissue excess (40 : 1), (2) use of 200 mM NH4Cl as a nuclease inhibitor, (3) addition of either sodium deoxycholate or Triton X−100 to the buffer before homogenization and (4) use of the Dounce homogenizer. Inclusion of NH4+ gives no deleterious effects with respect to dissociation or activity of the ribosomes.The occurrence of cold-induced ‘run-off’ of polysomes has been confirmed by direct measurement. Polysomes reassemble within 15 to 30 min after return of the animals to higher temperatures, with restoration of endogenous protein synthetic capacity to control levels; the ribosomes appear to retain an elevated capacity for poly(U)-directed protein synthesis. 相似文献
14.
Uzi Nur 《Chromosoma》1978,69(2):219-229
In grasshoppers, as well as in most other animals, the X chromosome is heteropycnotic (heterochromatic) during prophase I and metaphase I of spermatogenesis. During the same stages, in some of the cells of three Melanoplus femur-rubrum males (out of several hundred males examined) part of the X appeared euchromatic (E). In one male, the E segment was observed in 90% of the cells of a single cyst in which all the cells lacked one of the smallest autosomes. In another cyst of the same follicle all the cells contained one additional small autosome, and none of the Xs exhibited an E segment. The size of the E segment suggested that it resulted from the failure of part of the X to become heteropycnotic prior to the formation of the cyst. In the other two males, many of the cells contained chromosome fragments and translocations. In many cells in which the X exhibited an E segment, however, there was no evidence of chromosome breakage. The E segments were sometimes terminal and sometimes interstitial in the same cyst. This variation suggested that they resulted from the euchromatinization of part of the X immediately prior to prophase I of meiosis. Because fragmentation and the presence of Xs with an E segment were each very rare, it was concluded that they were in some way causally related. It was also concluded that in this species the heterochromatinization of the X is not controlled by a single inactivation center. 相似文献
15.
Additive Effects of Multiple SEGREGATION DISTORTER ( SD) Chromosomes on Sperm Dysfunction in DROSOPHILA MELANOGASTER 总被引:3,自引:3,他引:0
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Lyttle TW 《Genetics》1986,114(1):203-216
A portion of the Segregation distorter (SD) chromosome, including both the Sd and E(SD) loci, has been moved by insertional translocation from SD Roma into YL . This Dp(2;Y)SD chromosome shows a negligible reduction in its ability to cause dysfunction of Rsp s-bearing sperm when compared to the parent SD chromosome, suggesting that SD can still act effectively, even when removed from its normal second chromosome milieu, and that its activity level does not depend on pairing with a normal autosomal homologue. Male genotypes have been constructed using this Dp(2;Y)SD along with a standard SD chromosome (either SD Roma or R( SD-36)-1bw) and a third chromosome suppressor of SD (TM6) in all possible three-way combinations. The observed level of SD-mediated dysfunction in each case is most compatible with a model that assumes that all SD elements act additively (in terms of M, the probit transformation of the probability of sperm dysfunction), rather than multiplicatively. The additive action of SD elements contrasts with the independent response to SD activity exhibited by multiple Rsps copies. 相似文献
16.
D. G. Bedo 《Chromosoma》1980,77(3):299-308
In Lucilia cuprina C-banding produces procentric bands on all autosomes and deep staining over most of the X and Y chromosomes which conciderably facilitates the analysis of complex Y chromosome rearrangements. The Y chromosome is generally darkly C-banded throughout while in the X chromosome a pale staining segment is found in the distal portion of the long arm. Modulation of the banding reaction results in grey areas in both X and Y. When C-banding is compared with allocycly it is clear that not all heteropycnotic regions in the sex chromosomes C-band to the same extent. Secondary constrictions in the short arms of both X and Y chromosomes are clearly revealed by C-banding, the X satellite being polymorphic for size.— Q-banding results in a brightly fluorescing band in the short arm of structurally normal Y chromosomes. This band loses its fluorescence in some translocations, probably through a position effect. Hoechst 33258 staining does not produce any brightly fluorescing bands. 相似文献
17.
Kathie Y Sun Daniel Oreper Sarah A Schoenrock Rachel McMullan Paola Giusti-Rodríguez Vasyl Zhabotynsky Darla R Miller Lisa M Tarantino Fernando Pardo-Manuel de Villena William Valdar 《Genetics》2021,218(1)
Female mammals are functional mosaics of their parental X-linked gene expression due to X chromosome inactivation (XCI). This process inactivates one copy of the X chromosome in each cell during embryogenesis and that state is maintained clonally through mitosis. In mice, the choice of which parental X chromosome remains active is determined by the X chromosome controlling element (Xce), which has been mapped to a 176-kb candidate interval. A series of functional Xce alleles has been characterized or inferred for classical inbred strains based on biased, or skewed, inactivation of the parental X chromosomes in crosses between strains. To further explore the function structure basis and location of the Xce, we measured allele-specific expression of X-linked genes in a large population of F1 females generated from Collaborative Cross (CC) strains. Using published sequence data and applying a Bayesian “Pólya urn” model of XCI skew, we report two major findings. First, inter-individual variability in XCI suggests mouse epiblasts contain on average 20–30 cells contributing to brain. Second, CC founder strain NOD/ShiLtJ has a novel and unique functional allele, Xceg, that is the weakest in the Xce allelic series. Despite phylogenetic analysis confirming that NOD/ShiLtJ carries a haplotype almost identical to the well-characterized C57BL/6J (Xceb), we observed unexpected patterns of XCI skewing in females carrying the NOD/ShiLtJ haplotype within the Xce. Copy number variation is common at the Xce locus and we conclude that the observed allelic series is a product of independent and recurring duplications shared between weak Xce alleles. 相似文献
18.
When a dicentric chromosome breaks in mitosis, the broken ends cannot be repaired by normal mechanisms that join two broken ends since each end is in a separate daughter cell. However, in the male germline of Drosophila melanogaster, a broken end may be healed by de novo telomere addition. We find that Chk2 (encoded by lok) and P53, major mediators of the DNA damage response, have strong and opposite influences on the transmission of broken-and-healed chromosomes: lok mutants exhibit a large increase in the recovery of healed chromosomes relative to wildtype control males, but p53 mutants show a strong reduction. This contrasts with the soma, where mutations in lok and p53 have the nearly identical effect of allowing survival and proliferation of cells with irreparable DNA damage. Examination of testes revealed a transient depletion of germline cells after dicentric chromosome induction in the wildtype controls, and further showed that P53 is required for the germline to recover. Although lok mutant males transmit healed chromosomes at a high rate, broken chromosome ends can also persist through spermatogonial divisions without healing in lok mutants, giving rise to frequent dicentric bridges in Meiosis II. Cytological and genetic analyses show that spermatid nuclei derived from such meiotic divisions are eliminated during spermiogenesis, resulting in strong meiotic drive. We conclude that the primary responsibility for maintaining genome integrity in the male germline lies with Chk2, and that P53 is required to reconstitute the germline when cells are eliminated owing to unrepaired DNA damage. 相似文献
19.
Cytological identification of two X-chromosome types in the wood lemming (Myopus schisticolor) 总被引:1,自引:0,他引:1
Eberhard W. Herbst Karl Fredga Fritz Frank Heinz Winking Alfred Gropp 《Chromosoma》1978,69(2):185-191
In the wood lemming (Myopus schisticolor) three genetic types of sex chromosome constitution in females are postulated: XX, X*X and X*Y (X*=X with a mutation inactivating the male determining effect of the Y chromosome). Males are all XY. It is shown in the present paper that the two types of X chromosomes, X and X*, exhibit differences in the G-band patterns of their short arms. In addition, it was demonstrated in unbanded chromosomes that the short arm in X* is shorter than in X. The origin of these differences is still obscure; but they allow to identify and to distinguish the individual types of sex chromosome constitution, as of XX versus X*X females and of X*Y females versus XY males, on the basis of G-banded chromosome preparations from somatic cells. 相似文献
20.
B. Kiauta 《Genetica》1970,41(1):525-531
Epallage fatime (Charp.) is the first member of the family studied cytologically. The chromosome number is: 2n ♂=25,n ♂=13. The sex element is the smallest of the set at all stages of the spermatogenetic cycle. It is usually negatively heterocyclic at spermatogonial metaphase, whereas it is positively heteropyenotic at primary spermatocyte prophase and diakinesis. While the cytological similarities betweenEpallagidae, Hetaerinidae andCalopterygidae suggest their close mutual affinities, the three differ essentially from thePolythoridae. This view is only partly in agreement with the evidence on the structural and venational characters (ct.Fraser, 1954). Contrary toFraser's opinion (Fraser, 1957), thePseudolestidae can not be regarded, on the basis of the cytological information available, as an annectent family to the Calopterygoidea, but stand well apart from all other cytologically known Zygoptera. 相似文献