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小鼠、大鼠和兔体内的细胞色素P1 - 450结构基因:DNA甲基化及mRNA发育表达的差异

Cytochrome P1-450 structural gene in mouse, rat, and rabbit: differences in DNA methylation and developmental expression of mRNA.

作者信息

Chen Y T, Negishi M, Nebert D W

出版信息

DNA. 1982;1(3):231-8. doi: 10.1089/dna.1.1982.1.231.

Abstract

Clone 46 previously was shown to represent an 1100-bp cDNA clone of the mouse cytochrome P1-450 structural gene. Clone 46 [32P]DNA was hybridized to DNA and mRNA from mouse, rat, and rabbit of different ages. In Hpa II digests of DNA, two hybridizable fragments of less than 0.5 kb exist in adult "Ah-responsive" C57BL/6N mouse liver but not in C57BL/6N sperm or embryo or in adult "Ah-nonresponsive" DBA/2N mouse liver. The reason for this hypomethylation of adult C57BL/6N liver DNA is not known but might be related to the high degree of expressivity of this gene in adult C57BL/6N liver, compared with adult DBA/2N liver. No differences in Hpa II- or Msp I-digested DNA are seen in C57BL/6N or DBA/2N inbred strains treated with the P1-450 inducer, 3-methylcholanthrene (3-MC), versus untreated controls. The ontogenetic expression of 3-MC-induced P1-450 mRNA (23S) from mouse or rat liver corresponds well to previous developmental studies from this laboratory involving 3-MC-inducible aryl hydrocarbon (benzo[a]pyrene) hydroxylase (AHH) (EC 1.14.14.1) activity. P1-450 mRNA--induced transplacentally by 3-MC given to the mother--is readily detectable by clone 46 as early as gestational day 15. The cloned cDNA probe hybridizes to rat and rabbit DNA fragments of different sizes, and with less intensity, when compared with hybridization to mouse DNA. No hybridization of this DNA is observed with rabbit mRNA of all ages ranging from neonate to adult. These data suggest that sequence homology exists among the mouse, rat, and rabbit P1-450 structural genes and between mouse and rat P1-450 mRNA. The mouse cDNA probe is believed to hybridize to a segment of the rabbit P1-450 gene that is not transcribed.

摘要

克隆46先前已被证明代表小鼠细胞色素P1 - 450结构基因的一个1100碱基对的cDNA克隆。将克隆46 [³²P]DNA与来自不同年龄小鼠、大鼠和兔子的DNA及mRNA进行杂交。在DNA的Hpa II酶切片段中,成年“Ah反应型”C57BL/6N小鼠肝脏中存在两个小于0.5 kb的可杂交片段,而在C57BL/6N精子或胚胎中以及成年“Ah无反应型”DBA/2N小鼠肝脏中则不存在。成年C57BL/6N肝脏DNA这种低甲基化的原因尚不清楚,但可能与该基因在成年C57BL/6N肝脏中与成年DBA/2N肝脏相比具有高度的表达活性有关。在用P1 - 450诱导剂3 - 甲基胆蒽(3 - MC)处理的C57BL/6N或DBA/2N近交系中,与未处理的对照相比,在Hpa II或Msp I酶切的DNA中未观察到差异。来自小鼠或大鼠肝脏的3 - MC诱导的P1 - 450 mRNA(23S)的个体发育表达与本实验室先前涉及3 - MC诱导的芳烃(苯并[a]芘)羟化酶(AHH)(EC 1.14.14.1)活性的发育研究结果非常吻合。给母体注射3 - MC经胎盘诱导产生的P1 - 450 mRNA早在妊娠第15天就可被克隆46轻松检测到。与小鼠DNA杂交相比,该克隆的cDNA探针与不同大小的大鼠和兔子DNA片段杂交,且杂交强度较低。在从新生到成年的所有年龄段的兔子mRNA中均未观察到该DNA的杂交。这些数据表明,小鼠、大鼠和兔子的P1 - 450结构基因之间以及小鼠和大鼠的P1 - 450 mRNA之间存在序列同源性。据信,小鼠cDNA探针与兔子P1 - 450基因中未转录的一段序列杂交。

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