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首页> 外文期刊>Hereditas >Nonrandom de novo chromosome aberrations in human lymphocytes and amniotic cells
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Nonrandom de novo chromosome aberrations in human lymphocytes and amniotic cells

机译:人淋巴细胞和羊膜细胞的非随机新生染色体畸变

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The incidences and types of chromosome aberrations in single cells of individuals with a normal chromosome constitution were studied in two cell types, viz. lymphocytes and amniotic cells. A total of 17, 545 lymphocytes and 17, 262 amniotic cells were analyzed from 2, 554 consecutive individuals.The total incidence of numerical and structural aberrations was 2.0% and 1.6% in lymphocytes and amniotic cells, respectively. Two particular translocation types-t (7:14) (p 14–15; q 11–12) and t (7;14) (q 36: q 12)-were present in the lymphocytes of 1/145 individuals (1/1, 595 metaphases), whereas none of the amniotic cell metaphases displayed such a translocation. Otherwise, no apparent differences were found between the two cell types as regards incidences and types of numerical and structural aberrations.None of the structural aberrations found in lymphocytes and amniotic cells were identical to any of the consistent chromosome aberrations characteristics of malignant cells. The fact that the breakpoints in structural chromosome aberrations in isolated somatic cells seem to be basically different from these characteristic of neoplastic cells supports the conclusion that the cancer-associated aberrations are produced by mechanisms that actively favor the formation of such aberrations.
机译:在两种细胞类型中,研究了具有正常染色体组成的个体的单个细胞中染色体畸变的发生率和类型。淋巴细胞和羊膜细胞。从连续2,554名个体中共分析了17,545淋巴细胞和17,262羊水,其中淋巴细胞和羊水的数值和结构畸变的总发生率分别为2.0%和1.6%。 1/145个人的淋巴细胞中存在两种特殊的易位类型-t(7:14)(p 14-15; q 11-12)和t(7; 14)(q 36:q 12)(1 / 1、595个中期),而没有羊膜细胞中期显示出这种易位。否则,两种类型的细胞在发病率,数值和结构畸变的类型上都没有发现明显差异。淋巴细胞和羊膜细胞中发现的结构畸变均与恶性细胞的任何一致染色体畸变特征相同。分离的体细胞中结构染色体畸变的断点似乎与赘生性细胞的这些特征基本不同,这一事实支持以下结论:与癌症相关的畸变是由积极支持这种畸变形成的机制产生的。

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