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家隅蛛的染色体(蜘蛛目:漏斗蛛科) 总被引:3,自引:0,他引:3
报告家隅蛛的染色体数目、形态结构和性染色体组成。实验结果表明:家隅蛛的染色体数目是:雄性体细胞为43,雌体为46。性别决定机制是X_1X_2X_3O型。3个(对)X染色体是全部染色体中最小的和次最小的。所有染色体几乎都是端或亚端着丝粒染色体,这一结论被对其C-显带标本的分析所证实。6~#~14~#染色体长臂末端有明显的结构异染色质。G-显带标本中,获得了清晰的带纹。 相似文献
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Greilhuber J. 《TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik》1977,50(3):121-124
Summary Giemsa techniques have refused to reveal G-banding patterns in plant chromosomes. Whatever has been differentially stained so far in plant chromosomes by various techniques represents constitutive heterochromatin (redefined in this paper). Patterns of this type must not be confused with the G-banding patterns of higher vertebrates which reveal an additional chromosome segmentation beyond that due to constitutive heterochromatin. The absence of G-bands in plants is explained as follows: 1) Plant chromosomes in metaphase contain much more DNA than G-banding vertebrate chromosomes of comparable length. At such a high degree of contraction vertebrate chromosomes too would not show G-bands, simply for optical reasons. 2) The striking correspondence of pachytene chromomeres and mitotic G-bands in higher vertebrates suggests that pachytene chromomeres are G-band equivalents, and that this may also be the case in plants. G-banded vertebrate chromosomes are on the average only 2.3 times shorter in mitosis than in pachytene; the chromomeric pattern therefore still can be shown. In contrast, plant chromosomes are approximately 10 times shorter at mitotic metaphase; their pachytene-like arrangement of chromomeres is therefore no longer demonstrable. 相似文献
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Inverted duplications associated with terminal deletions are complex anomalies described in an increasing of chromosome ends. We report on the cytogenetic characterization of the first de novo inv dup del(4) with partial 4p duplication and 4q deletion in a girl with clinical signs consistent with “recombinant 4 syndrome”. This abnormality was suspected by banding, but high-resolution molecular cytogenetic investigations allowed us to define the breakpoints of the rearrangement. The terminal duplicated region extending from 4p15.1 to the telomere was estimated to be 29.27 Mb, while the size of the terminal deletion was 3.114 Mb in the 4q35.1 region. Until now, 10 patients with duplicated 4p14-p15 and deleted 4q35 chromosome 4 have been described. In all cases the abnormal chromosome 4 was derived from a pericentric inversion inherited from one of the parents. In conclusion, we have identified the first case of inv dup del(4) with normal parents suggesting that, often, terminal duplications or terminal deletions mask complex rearrangements. 相似文献
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不同添加物质对香烟烟雾水溶物引起的蚕豆根尖细胞微核率的影响 总被引:13,自引:3,他引:13
本课题研究了不同添加物质对香烟烟雾水溶物引起的蚕豆根尖细胞微核率的影响。结果表明亚硒酸钠、烟酰胺、绿茶浸出物和维生素C均能显著降低由香烟烟雾水溶物引起的微核率,上述物质可能具有减轻吸烟引起的遗传毒性损伤的作用。此外,本文还对上述结果的意义进行了讨论。 相似文献
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Angel E. Spotorno Juan C. Marin Marco Yévenes Laura I. Walker Raúl Fernández-Donoso Juana Pincheira M. Soledad Berríos R. Eduardo Palma 《Journal of Mammalian Evolution》1997,4(4):259-269
To investigate the phylogenetic relationships of living marsupials, morphometric and G-banded chromosome analyses were made in the Chilean species Dromiciops gliroides (Microbiotheria) and Thylamys elegans (Didelphimorphia). Chromosome arm lengths and patterns of G-bands were compared in at least eight bone marrow metaphase spreads in six and nine specimens, respectively. They were contrasted with those published for another 11 American and Australian genera. Three of six autosomal pairs (A1, A3, and C2) were uniquely shared by Dromiciops and some Australian species, being different in shape and G-banded patterns from those with similar total sizes in Thylamys and other South American didelphoid karyotypes. Such chromosomal correspondences suggest the past occurrence of at least three pericentric inversions. A table of character states constructed from chromosomal G-band comparisons is presented, showing that cytogenetic data agree with Szalay's (1982) hypothesis on the affinities of the South American Dromiciops with Australian marsupials. 相似文献
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C. Sismani J. Donoghue A Alexandrou M. Karkaletsi S. Christopoulou A.E. Konstantinidou P. Livanos P.C. Patsalis V. Velissariou 《Gene》2013
Duplications of the X chromosome are rare cytogenetic findings, and have been associated with an abnormal phenotype in the male offspring of apparently normal or near normal female carriers. We report on the prenatal diagnosis of a duplication on the long arm of chromosome X from chromosomal band Xq13.2 to q21.31 in a male fetus with increased nuchal translucency in the first trimester and polyhydramnios at 22 weeks of gestation. Amniocentesis was undertaken and cytogenetic analysis revealed additional chromosomal material in the long arm of chromosome X at position Xq13. Analysis with high resolution array CGH revealed the additional material is in fact a duplication of the region Xq13.2–q21.13. The duplication is 14.8 Mb in size and includes fourteen genes: SLC16A2, KIAA2022, ABCB7, ZDHHC15, ATRX, MAGT1, ATP7A, PGK1, TBX22, BRWD3, POU3F4, ZNF711, POF1B and CHM. Analysis of the parents revealed the mother to be a carrier of the same duplication. After elected termination of the pregnancy at 28 weeks a detailed autopsy of the fetus allowed for genotype–phenotype correlations. 相似文献
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Arelí López-Uriarte Fabiola Quintero-Rivera Beatriz de la Fuente Cortez Viviana Gómez Puente María del Roble Velazco Campos Laura E. Martínez de Villarreal 《Gene》2013
We report here a child with a ring chromosome 2 [r(2)] associated with failure to thrive, microcephaly and dysmorphic features. The chromosomal aberration was defined by chromosome microarray analysis, revealing two small deletions of 2p25.3 (139 kb) and 2q37.3 (147 kb). 相似文献
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