Cantú E S, Nussbaum R L, Airhart S D, Ledbetter D H
Am J Hum Genet. 1985 Sep;37(5):947-55.
Thymidylate synthase (TS) activity was monitored in fluorodeoxyuridine (FUdR)-treated lymphoblasts from individuals carrying the fragile (X) [fra(X)] chromosome. Fra(X) expression and levels of TS activity were measured over a 72-hr period at different cell densities. TS activity was 80%-90% inhibited immediately after exposure to FUdR and remained suppressed for the first 24 hrs. Fra(X) expression was not found until 6-8 hrs after FUdR treatment, and at 24 hrs, reached a maximum expression of approximately 50%. At 48 and 72 hrs, however, increasing levels of TS activity paralleled a dramatic drop in fra(X) expression. High fra(X) expression at 48 and 72 hrs could be maintained by rechallenging cultures with increasing doses of FUdR. At low cell densities, fra(X) expression was maintained at high levels for a much longer period of time. In two lymphoblastoid cell lines from obligate carriers, which either expressed at very low levels or did not express the fra(X) in routine cultures, TS activity was also 90% inhibited but with no corresponding fra(X) expression 12 or 24 hrs after FUdR treatment. We conclude that: FUdR inhibits TS activity immediately and induces fra(X) expression 6-8 hrs later, FUdR-induced fra(X) expression and TS activity are inversely related, the FUdR effect on fra(X) expression and TS activity is time and cell-density dependent, and inhibition of TS activity is a necessary but not sufficient condition for fra(X) expression.
在来自携带脆性X染色体[fra(X)]个体的经氟脱氧尿苷(FUdR)处理的淋巴母细胞中监测胸苷酸合成酶(TS)活性。在不同细胞密度下,在72小时内测量fra(X)表达和TS活性水平。暴露于FUdR后,TS活性立即被抑制80%-90%,并在最初24小时内保持受抑制状态。直到FUdR处理后6-8小时才发现fra(X)表达,在24小时时,达到约50%的最大表达。然而,在48和72小时时,TS活性水平的增加与fra(X)表达的急剧下降平行。通过用增加剂量的FUdR再次刺激培养物,可以在48和72小时维持高fra(X)表达。在低细胞密度下,fra(X)表达在更长时间内维持在高水平。在来自 obligate携带者的两个淋巴母细胞系中,它们在常规培养中要么表达水平非常低,要么不表达fra(X),在FUdR处理后12或24小时,TS活性也被抑制90%,但没有相应的fra(X)表达。我们得出结论:FUdR立即抑制TS活性,并在6-8小时后诱导fra(X)表达;FUdR诱导的fra(X)表达与TS活性呈负相关;FUdR对fra(X)表达和TS活性的影响取决于时间和细胞密度;TS活性的抑制是fra(X)表达的必要但不充分条件。