Wirth P J, Fujimoto Y, Takahashi H, Mori M, Yoshida M C, Sugimura T, Nagao M
Carcinogenesis Division, National Cancer Center Research Institute, Tokyo.
Jpn J Cancer Res. 1990 May;81(5):477-82. doi: 10.1111/j.1349-7006.1990.tb02594.x.
High-resolution two-dimensional polyacrylamide gel electrophoresis in combination with silver staining was used to analyze between 800 and 1000 cytosolic and particulate polypeptides from age-matched livers of normal male Long-Evans rat with Agouti coat color (LEA) and Long-Evans rat with Cinnamon-like coat color (LEC) rats with hereditary trait of hepatitis at ages long before, immediately prior to, and just after the onset of hepatitis. Although the electrophoretic patterns of polypeptide expression were very similar with respect to the overall spot patterns, a number of polypeptides which differed either qualitatively or quantitatively were noted. Two constitutively expressed cytosolic polypeptides, P29.5 (Mr 29.5 kDa/pI 6.73) and P30 (30 kDa/6.70), were not detected in livers of LEC animals at any age. In the normal LEA rats both P29.5 and P30 were detected as early as one day after birth and both were expressed at similar concentrations at all ages. In the LEC rats P30-C (30 kDa/6.68) was constitutively expressed in close proximity to the expected position of P30, and P30-C was not detected in the LEA rats. By means of non-equilibrium pH gradient electrophoresis two relatively basic polypeptides were detected in the LEC rats. P18ne was detected immediately prior to and P27ne immediately after the clinical manifestation of hepatitis. Experiments in F1 backcross ([LEA x LEC] x LEC) animals, however, failed to demonstrate any genetic link between either the expression or lack of expression of P29.5, P30, P30-C, or P18ne and hepatitis development. P27ne was detected in all backcross animals exhibiting hepatitis, but was never observed in LEC rats prior to the onset of hepatitis. Although we were unable to identify any unique loss of expression of polypeptides which are genetically linked to hepatitis susceptibility in LEC rats, specific subsets of quantitatively modulated polypeptides were detected.
采用高分辨率二维聚丙烯酰胺凝胶电泳结合银染法,对毛色为刺豚鼠色的正常雄性长 Evans 大鼠(LEA)和具有类似肉桂色毛色且有遗传性肝炎特征的长 Evans 大鼠(LEC)在肝炎发病前很久、即将发病时以及发病后不久的年龄匹配肝脏中的 800 至 1000 种胞质和颗粒多肽进行分析。尽管多肽表达的电泳图谱在整体斑点模式方面非常相似,但注意到一些多肽在定性或定量上存在差异。两种组成性表达的胞质多肽,P29.5(分子量 29.5 kDa/等电点 6.73)和 P30(30 kDa/6.70),在任何年龄的 LEC 动物肝脏中均未检测到。在正常的 LEA 大鼠中,P29.5 和 P30 早在出生后一天就被检测到,并且在所有年龄段都以相似的浓度表达。在 LEC 大鼠中,P30-C(30 kDa/6.68)在紧邻 P30 预期位置处组成性表达,而在 LEA 大鼠中未检测到 P30-C。通过非平衡 pH 梯度电泳,在 LEC 大鼠中检测到两种相对碱性的多肽。P18ne 在肝炎临床表现前立即被检测到,P27ne 在肝炎临床表现后立即被检测到。然而,在 F1 回交([LEA×LEC]×LEC)动物中的实验未能证明 P29.5、P30、P30-C 或 P18ne 的表达或不表达与肝炎发展之间存在任何遗传联系。P27ne 在所有表现出肝炎的回交动物中均被检测到,但在 LEC 大鼠肝炎发病前从未观察到。尽管我们无法确定与 LEC 大鼠肝炎易感性存在遗传联系的多肽表达的任何独特缺失,但检测到了定量调节多肽的特定子集。