Babu A, Verma R S, Patil S R
Chromosoma. 1987;95(3):163-6. doi: 10.1007/BF00330345.
The pericentric chromatin of chromosome 18 was found to be far more heterogeneous for restriction endonuclease AluI (5'...AG decrease CT...3') than previously thought. The extent of such heterogeneity was characterized using 50 normal Caucasians and 5 cases of trisomy 18 or Edwards' Syndrome. The AluI-resistant chromatin can arbitrarily be classified into at least five sizes by comparison with the length of the short arm (p) of chromosome 18. They are: negative (1), small (2), medium (3), large (4) and very large (5) with incidences of 11.30%, 19.13%, 29.57%, 29.57% and 10.43%, respectively. In addition the location of the chromatin can be classified into four types depending upon the position relative to the primary constriction. For example: Type I (absent); Type II (present on p arm only); Type III (present on q arm only); Type IV (present on centromere and extending into both p and q arms). The incidences of types I, II, III, and IV were 11.30%, 62.61%, 0.87%, and 25.22%, respectively. Based on limited data, AluI-resistant chromatin was found to be predominantly "large" and "very large" in Edwards' Syndrome samples. In addition, no case with negative Alu-resistant chromatin was noted. Therefore, it is tempting to speculate that the amount of chromatin present on the centromere might play a role in non-disjunction in Edwards' Syndrome cases. Although the variation observed in the present study is continuous, the proposed classification has some important implications for future investigations.
研究发现,18号染色体的着丝粒周围染色质对限制性内切酶AluI(5'...AG↓CT...3')的敏感性远比之前认为的要异质得多。利用50名正常白种人和5例18三体或爱德华兹综合征患者,对这种异质性的程度进行了表征。通过与18号染色体短臂(p)的长度比较,AluI抗性染色质可任意分为至少五种大小。它们分别是:阴性(1)、小(2)、中(3)、大(4)和非常大(5),发生率分别为11.30%、19.13%、29.57%、29.57%和10.43%。此外,根据染色质相对于主缢痕的位置,其位置可分为四种类型。例如:I型(无);II型(仅存在于p臂);III型(仅存在于q臂);IV型(存在于着丝粒并延伸至p臂和q臂)。I型、II型、III型和IV型的发生率分别为11.30%、62.61%、0.87%和25.22%。基于有限的数据,在爱德华兹综合征样本中发现AluI抗性染色质主要为“大”和“非常大 ”。此外,未发现有阴性Alu抗性染色质的病例。因此,很容易推测着丝粒上存在的染色质数量可能在爱德华兹综合征病例的不分离过程中起作用。尽管本研究中观察到的变异是连续的,但所提出的分类对未来的研究具有一些重要意义。