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1.
The chromosomes of first cleavage mouse embryos show the same banding patterns after quinacrine mustard staining as do chromosomes of differentiated mouse cells. Whatever feature of chromosome structure the banding pattern reveals thus appears not to be altered during development and differentiation. 相似文献
2.
Chromosomal localization of mouse satellite DNA 总被引：67，自引：0，他引：67
Hybridization of radioactive nucleic acids with the DNA of cytological preparations shows that the sequences of mouse satellite DNA are located in the centromeric heterochromatin of the mouse chromosomes. Other types of heterochromatin in the cytological preparations do not contain satellite DNA. 相似文献
3.
X-Chromosome inactivation in cloned mouse embryos 总被引：2，自引：0，他引：2
Eggan K Akutsu H Hochedlinger K Rideout W Yanagimachi R Jaenisch R 《Science (New York, N.Y.)》2000,290(5496):1578-1581
To study whether cloning resets the epigenetic differences between the two X chromosomes of a somatic female nucleus, we monitored X inactivation in cloned mouse embryos. Both X chromosomes were active during cleavage of cloned embryos, followed by random X inactivation in the embryo proper. In the trophectoderm (TE), X inactivation was nonrandom with the inactivated X of the somatic donor being chosen for inactivation. When female embryonic stem cells with two active X chromosomes were used as donors, random X inactivation was seen in the TE and embryo. These results demonstrate that epigenetic marks can be removed and reestablished on either X chromosome during cloning. Our results also suggest that the epigenetic marks imposed on the X chromosomes during gametogenesis, responsible for normal imprinted X inactivation in the TE, are functionally equivalent to the marks imposed on the chromosomes during somatic X inactivation. 相似文献
4.
A fluorescent staining technique has demonstrated a contralateral arrangement of fluorescent spots in the centromeric region of mouse metacentric chromosomes which have resulted from centric fusion. The results suggest that centric fusion involves the maintenance of DNA polaritv through the centromere and that the thymidine-rich chain of satellite DNA in the centromeric region is associated with the same DNA chain in every mouse autosome. 相似文献
5.
Linkage groups II and XII of the mouse: cytological localization by fluorochrome staining 总被引：1，自引：0，他引：1
The T(2;12) 163H translocation involves two chromosomes which carry the two groups of genes known as linkage groups II and XII. Staining with quinacrine mustard reveals that these chromosomes are numbers 10 and 19 of the fluorescent karyotype of the normal mouse. Linkage group II is assigned to chromosome 10, linkage group XII to chromosome 19. 相似文献
6.
Chromosome mapping in the mouse, fluorescence banding techniques permit assignment of most genetic linkage groups 总被引：1，自引：0，他引：1
Chromosome banding techniques have permitted the identification of every normal chromosome in the mouse, Mus musculus, and the demonstration of strain differences. By identifying the chromosomes involved in a series of translocations, it has been possible to assign 14 of the 19 known linkage groups to 14 different chromosomes. These powerful cytological methods promise to revolutionize cytogenetic studies in higher organisms. 相似文献
7.
Duplication, deletion, and polymorphism in the sex-determining region of the mouse Y chromosome 总被引：13，自引：0，他引：13
G Mardon R Mosher C M Disteche Y Nishioka A McLaren D C Page 《Science (New York, N.Y.)》1989,243(4887):78-80
The ZFY gene in the sex-determining region of the human Y chromosome encodes a "zinc-finger" protein that may be the testis-determining factor, TDF. Although the Y chromosomes of most placental mammals carry a single homolog of ZFY, the mouse Y chromosome has two homologs, both in the sex-determining (Sxr) region. Zfy-1 alone may suffice to determine maleness; Zfy-2 is dispensable, as it was deleted in an Sxr variant that retains sex-determining function but has lost other genes. Both loci mapped near the centromere of the mouse Y chromosome. The Y chromosomes of the subspecies Mus musculus musculus and M. m. domesticus were distinguishable by a Zfy-1 restriction fragment polymorphism, which can be used to study their differing interactions with autosomal sex-determining genes. 相似文献
8.
G Jagiello 《Science (New York, N.Y.)》1967,157(787):453-454
Streptonigrin, an antibiotic and antitumor agent, alters the chromosomes of the mouse ovum during meiosis. Agglutination of bivalents or achromatic gaps and breaks occurred in the larger pairs both in vitro and in vivo. This newly detected cytogenetic effect suggests that such agents can gain access to developing mammalian ova and destroy the normal progress of meiosis. 相似文献
9.
Organization of the human and mouse low-affinity Fc gamma R genes: duplication and recombination 总被引：19，自引：0，他引：19
W Q Qiu D de Bruin B H Brownstein R Pearse J V Ravetch 《Science (New York, N.Y.)》1990,248(4956):732-735
Receptors for immunoglobulin G immune complexes (Fc gamma RII and Fc gamma RIII) are expressed on most hematopoietic cells and show much structural and functional diversity. In order to determine the genetic basis for this diversity, a family of genes encoding the human and mouse receptors was isolated and characterized. Humans have five distinct genes for low-affinity Fc gamma Rs, in contrast to two in the mouse. With the use of yeast artificial chromosomes, the genes encoding the human receptors were oriented and linked, which established the structure of this complex locus. Comparison of the human and mouse genes generated a model for the evolutionary amplification of this locus. 相似文献
10.
Somatic cell hybrid between the established human line D98 (presumptive HeLa) and 3T3 总被引：15，自引：0，他引：15
Somatic cell hybrids have been made between an established human cell line with a long culture history and established mouse fibroblast line. When first analyzed, the hybrid cells contained nearly twice as many mouse chromosomes as the mouse parent line and a human chromosome complemnent of about half that of the human parent. There was further loss of human chromosomes on continued cultivation. This behavior resembles that of other human mouse hybrids and appears to be characteristic of the human-mouse combination. However, the number of human chromosomes is greater than in hybrids made from human diploid fibroblasts. Some clones contain more than a haptoid quantity of human DNA per cell and should synthesize a much greater number of human gene products. 相似文献
11.
Haber JE 《Science (New York, N.Y.)》2006,313(5790):1045; author reply 1045
Armakolas and Klar (Reports, 24 February 2006, p. 1146) suggested that segregation of mouse chromosome 7, after induction of a site-specific crossover between homologous chromosomes, is driven by a preferential inheritance of the old Watson and the old Crick DNA strands. However, this interpretation only considered half of the possible outcomes. The conjecture fails when all possible outcomes are examined. 相似文献
12.
Inactivation of one of the two X chromosomes occurs in all cells of female adult mice so that genes are expressed from only one X chromosome. In a Perspective, Clerc and Avner describe an elegant series of experiments in mouse embryos cloned from adult and embryonic female cell nuclei (Eggan et al.) that reveal how the inactivation state of the X chromosomes is reprogrammed. 相似文献
13.
C J Epstein 《Science (New York, N.Y.)》1972,175(29):1467-1468
The activity of hypoxanthine-guanine phosphoribosyltransferase in unfertilized mouse ova and in mouse embryos at the two-cell stage is proportional to the number of X chromosomes present during oogenesis. This indicates that the enzyme is X-linked in the mouse and that inactivation of the X chromosome does not occur during oogenesis. However, the genetic dosage effect of the X chromosomes is not present after the increase in hypoxanthine-guanine phosphoribosyltransferase activity in the late morula and the blastocyst stages. These results indicate that the X-linked enzyme lacuts is expressed sometimne after fertilization but before the morula stage. 相似文献
14.
Williams BR Prabhu VR Hunter KE Glazier CM Whittaker CA Housman DE Amon A 《Science (New York, N.Y.)》2008,322(5902):703-709
Aneuploidy, an incorrect number of chromosomes, is the leading cause of miscarriages and mental retardation in humans and is a hallmark of cancer. We examined the effects of aneuploidy on primary mouse cells by generating a series of cell lines that carry an extra copy of one of four mouse chromosomes. In all four trisomic lines, proliferation was impaired and metabolic properties were altered. Immortalization, the acquisition of the ability to proliferate indefinitely, was also affected by the presence of an additional copy of certain chromosomes. Our data indicate that aneuploidy decreases not only organismal but also cellular fitness and elicits traits that are shared between different aneuploid cells. 相似文献
15.
Stable antibody-producing murine hybridomas 总被引：24，自引：0，他引：24
A method is described for obtaining antibody-producing hybridomas that are preferentially retained in cultures of fused mouse spleen and myeloma cells. Hybridomas are produced by fusing mouse myeloma cells that are deficient in adenosine phosphoribosyltransferase (APRT) with mouse spleen cells containing Robertsonian 8.12 translocation chromosomes. The cell fusion mixtures are exposed to a culture medium that can be utilized only by APRT-positive cells, which results in the elimination of both unfused APRT-deficient myeloma cells and non-antibody-producing APRT-deficient hybridomas that arise by segregation of the 8.12 translocation chromosomes containing the APRT genes and the active heavy chain immunoglobulin gene. 相似文献
16.
Chromosomal locations of the murine T-cell receptor alpha-chain gene and the T-cell gamma gene 总被引：11，自引：0，他引：11
D M Kranz H Saito C M Disteche K Swisshelm D Pravtcheva F H Ruddle H N Eisen S Tonegawa 《Science (New York, N.Y.)》1985,227(4689):941-945
Two independent methods were used to identify the mouse chromosomes on which are located two families of immunoglobulin (Ig)-like genes that are rearranged and expressed in T lymphocytes. The genes coding for the alpha subunit of T-cell receptors are on chromosome 14 and the gamma genes, whose function is yet to be determined, are on chromosome 13. Since genes for the T-cell receptor beta chain were previously shown to be on mouse chromosome 6, all three of the Ig-like multigene families expressed and rearranged in T cells are located on different chromosomes, just as are the B-cell multigene families for the Ig heavy chain, and the Ig kappa and lambda light chains. The findings do not support earlier contentions that genes for T-cell receptors are linked to the Ig heavy chain locus (mouse chromosome 12) or to the major histocompatibility complex (mouse chromosome 17). 相似文献
17.
F A McMorris T R Chen F Ricciuti J Tischfield R Creagan F Ruddle 《Science (New York, N.Y.)》1973,179(78):1129-1131
Thirty-seven clones of somatic cell hybrids between human and mouse cells were examined for retention of human chromosomes and expression of human constitutive enzymes. Human glucosephosphate isomerase and chromosome F-19 were retained or lost concordantly, as were human mannosephosphate isomerase and chromosome C-7. The genes for the enzymes are thus assigned to these two chromosomes. 相似文献
18.
Sensing X chromosome pairs before X inactivation via a novel X-pairing region of the Xic 总被引：1，自引：0，他引：1
Augui S Filion GJ Huart S Nora E Guggiari M Maresca M Stewart AF Heard E 《Science (New York, N.Y.)》2007,318(5856):1632-1636
19.
The active exogenous murine leukemia virus sequences of mouse cells growing in culture are preferentially digested by deoxyribonuclease I in metaphase chromosomes. As determined by nuclear nick translation, all of the gene sequences of these cells active during interphase are in a deoxyribonuclease I-sensitive conformation during metaphase. This method of nick translation can therefore be used to label chromosomes in situ in order to visualize the active regions of the genome. 相似文献
20.
The rapidly labeled RNA from both the nuclei and cytoplasm of mouse liver cells can be bound specifically to mouse DNA. The bound fraction differs in base composition and metabolic stability from the bulk RNA. There is considerable cross reaction between this RNA and the DNA obtained from calf thymus. 相似文献