Expression of Brca1 and splice variant Brca1Δ11 RNA levels in mouse mammary gland during normal development and tumorigenesis

被引:20
作者
Mixon, M [1 ]
Kittrell, F [1 ]
Medina, D [1 ]
机构
[1] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
关键词
genes; Brca1; breast neoplasms; gene expression;
D O I
10.1038/sj.onc.1203905
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Expression of Brca1 in mouse mammary cancer has yet to be analysed. We use a progressive model of neoplasia based on several mouse epithelial cell lines that represent distinct steps toward the fully tumorigenic state. Using RNase protection analysis because acceptable anti-Brca1 antibodies are not available we investigated the expression of Brca1 and a splice variant, Brca1 Delta 11, in several mammary hyperplasias and tumors that arose from them, and in normal mammary gland through pregnancy and involution, Expression of Brca1 was highest in rapidly proliferating cells. Expression of the full-length Brca1 was detectable in the virgin gland, was slightly elevated in the midpregnant gland, and decreased to levels similar to the age-matched virgin gland in the completely involuted gland, Expression of both forms of Brca1 was detectable in 9/9 paired hyperplasias and tumors, with levels of total Brca1, but not the splice variant Brca1 Delta 11, in tumors higher than those in the hyperplasias. While in disagreement with the observation that Brca1 levels decrease in human breast cancer progression, these patterns support the notion that Brca1 expression is associated with proliferating cells, and suggests that the link with differentiation seen in normal cells can be removed when cells become tumorigenic.
引用
收藏
页码:5237 / 5243
页数:7
相关论文
共 37 条
[1]   BRCA1 expression restores radiation resistance in BRCA1-defective cancer cells through enhancement of transcription-coupled DNA repair [J].
Abbott, DW ;
Thompson, ME ;
Robinson-Benion, C ;
Tomlinson, G ;
Jensen, RA ;
Holt, JT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (26) :18808-18812
[2]   Brca1 and Brca2 expression patterns in mitotic and meiotic cells of mice. [J].
Blackshear, PE ;
Goldsworthy, SM ;
Foley, JF ;
McAllister, KA ;
Bennett, LM ;
Collins, NK ;
Bunch, DO ;
Brown, P ;
Wiseman, RW ;
Davis, BJ .
ONCOGENE, 1998, 16 (01) :61-68
[3]   A superfamily of conserved domains in DNA damage responsive cell cycle checkpoint proteins [J].
Bork, P ;
Hofmann, K ;
Bucher, P ;
Neuwald, AF ;
Altschul, SF ;
Koonin, EV .
FASEB JOURNAL, 1997, 11 (01) :68-76
[4]   From BRCA1 to RAP1: A widespread BRCT module closely associated with DNA repair [J].
Callebaut, I ;
Mornon, JP .
FEBS LETTERS, 1997, 400 (01) :25-30
[5]  
Chen YM, 1996, CANCER RES, V56, P3168
[6]  
EASTON D, 1993, CANCER SURV, V18, P95
[7]   Brca1 deficiency results in early embryonic lethality characterized by neuroepithelial abnormalities [J].
Gowen, LC ;
Johnson, BL ;
Latour, AM ;
Sulik, KK ;
Koller, BH .
NATURE GENETICS, 1996, 12 (02) :191-194
[8]   RETRACTED: BRCA1 required for transcription-coupled repair of oxidative DNA damage (Retracted article. See vol 300, pg 1657, June 13 2003) [J].
Gowen, LC ;
Avrutskaya, AV ;
Latour, AM ;
Koller, BH ;
Leadon, SA .
SCIENCE, 1998, 281 (5379) :1009-1012
[9]  
Husain A, 1998, CANCER RES, V58, P1120
[10]   Immortalized mouse mammary cells in vivo do not exhibit increased telomerase activity [J].
Jiang, C ;
Juo, L ;
Said, TK ;
Thompson, H ;
Medina, D .
CARCINOGENESIS, 1997, 18 (11) :2085-2091