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C3Hf/Ki小鼠的乳腺肿瘤发生:对生殖系小鼠乳腺肿瘤病毒以及int-1和int-2假定原癌基因的检测

Mammary tumorigenesis in C3Hf/Ki mice: examination of germinal mouse mammary tumor viruses and the int-1 and int-2 putative proto-oncogenes.

作者信息

Popko B J, Pauley R J

出版信息

Virus Res. 1985 Apr;2(3):231-43. doi: 10.1016/0168-1702(85)90011-5.

Abstract

The organization and expression of endogenous mouse mammary tumor virus (MMTV) proviruses in normal and neoplastic C3Hf/Ki tissues were examined. MMTV-containing EcoRI, HindIII, BamHI and PstI restriction fragments of C3Hf/Ki DNA were identical to those of C3H/StWi DNA. The full-length endogenous MMTV Units Ia (Mtv-7), II (Mtv-8), III (Mtv-9) and IV (Mtv-10), in addition to the subgenomic endogenous MMTV Units I (Mtv-6) and IX (Mtv-14), were germinally transmitted in C3Hf/Ki DNA. The previously uncharacterized Mtv-7 was contained in EcoRI fragments of 16.7 and 11.7 kbp. The endogenous MMTV Unit V (Mtv-1), which is responsible for virus production and mammary tumorigenesis in C3Hf/He mice, was absent from C3Hf/Ki DNA. The 9.0 kb gag-pol, the 3.8 kb env and the 1.7 kb LTR MMTV RNA transcripts were present in C3Hf/Ki mammary glands. MMTV proviruses, in addition to the endogenous C3Hf/Ki MMTV complement, were not detected in C3Hf/Ki mammary tumor DNA. The DNA organization and RNA expression of the putative mammary proto-oncogene regions int-1 and int-2 were also examined in C3Hf/Ki mammary tumors. The int-1 and int-2 regions did not appear rearranged, amplified, or expressed in C3Hf/Ki mammary tumors. These studies indicate that MMTV proviral activation of the int proto-oncogenes is not necessary for C3Hf/Ki mammary tumorigenesis.

摘要

研究了内源性小鼠乳腺肿瘤病毒(MMTV)前病毒在正常和肿瘤性C3Hf/Ki组织中的组织形式和表达情况。C3Hf/Ki DNA中含MMTV的EcoRI、HindIII、BamHI和PstI限制性片段与C3H/StWi DNA的片段相同。除亚基因组内源性MMTV单元I(Mtv-6)和IX(Mtv-14)外,全长内源性MMTV单元Ia(Mtv-7)、II(Mtv-8)、III(Mtv-9)和IV(Mtv-10)在C3Hf/Ki DNA中可通过生殖系传递。先前未鉴定的Mtv-7存在于16.7和11.7 kbp的EcoRI片段中。在C3Hf/Ki DNA中不存在负责C3Hf/He小鼠病毒产生和乳腺肿瘤发生的内源性MMTV单元V(Mtv-1)。9.0 kb的gag-pol、3.8 kb的env和1.7 kb的LTR MMTV RNA转录本存在于C3Hf/Ki乳腺组织中。在C3Hf/Ki乳腺肿瘤DNA中未检测到除内源性C3Hf/Ki MMTV互补序列外的MMTV前病毒。还在C3Hf/Ki乳腺肿瘤中检测了假定的乳腺原癌基因区域int-1和int-2的DNA组织形式和RNA表达。在C3Hf/Ki乳腺肿瘤中,int-1和int-2区域未出现重排、扩增或表达。这些研究表明,MMTV前病毒激活int原癌基因对于C3Hf/Ki乳腺肿瘤发生并非必要条件。

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