TY - JOUR
T1 - Prediction of transcriptional activity based on gene association with the nuclear matrix
AU - Buttyan, Ralph
AU - Olsson, Carl A.
N1 - Funding Information:
We thank Z. Zakeri and D. Wolgemuth for their helpful criticism and stimulating discussion. This investigation was supported by a grant from the National Institutes of Health (5R23 AM3480).
PY - 1986/8/14
Y1 - 1986/8/14
N2 - In this report, we show that androgen-dependent genes expressed in rat ventral prostate, Cl, C2 and C3, are enriched in residual DNA extracted from the nuclear matrix of ventral prostate. The enrichment is androgen-dependent and is likely to be related to their transcriptional activity. While this finding corroborates other data demonstrating that transcriptionally active genes can be protected from nuclease digestion by their association with the nuclear matrix, we have extended this analysis to show that nuclear matrix protection experiments can be used both to analyze tissue-specific expression among members of a highly related gene family and also to predict transcriptional activity of genes in particular tissues.
AB - In this report, we show that androgen-dependent genes expressed in rat ventral prostate, Cl, C2 and C3, are enriched in residual DNA extracted from the nuclear matrix of ventral prostate. The enrichment is androgen-dependent and is likely to be related to their transcriptional activity. While this finding corroborates other data demonstrating that transcriptionally active genes can be protected from nuclease digestion by their association with the nuclear matrix, we have extended this analysis to show that nuclear matrix protection experiments can be used both to analyze tissue-specific expression among members of a highly related gene family and also to predict transcriptional activity of genes in particular tissues.
UR - http://www.scopus.com/inward/record.url?scp=0022521506&partnerID=8YFLogxK
U2 - 10.1016/S0006-291X(86)80429-6
DO - 10.1016/S0006-291X(86)80429-6
M3 - Article
C2 - 3753498
AN - SCOPUS:0022521506
VL - 138
SP - 1334
EP - 1340
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
SN - 0006-291X
IS - 3
ER -