TY - JOUR
T1 - A maize Myb homolog is encoded by a multicopy gene complex
AU - Chopra, S.
AU - Athma, P.
AU - Li, X. G.
AU - Peterson, T.
N1 - Funding Information:
Acknowledgements We thank Karen Price and Edwards Allen for assistance with isolation and analysis of k genomic clones, and Suzy Cocciolone for valuable suggestions. This research was supported by grants from the Department of Energy and the National Science Foundation. Journal Paper No. J-17726 of the Iowa Agriculture and Home Economics Experiment Station, Ames, Iowa. Project No. 3297, and supported by Hatch Act and State of Iowa funds. The experiments reported herein comply with the current laws of the United States of America.
PY - 1998
Y1 - 1998
N2 - The maize P gene encodes a Myb-homologous transcriptional regulator of flavonoid pigmentation in floral organs, and different P gene alleles condition precise tissue- and organ-specific pigmentation patterns. To determine the molecular basis for allele-specific expression patterns, we have isolated and compared two natural alleles of the P gene which differ in expression, structure and copy number. The P-rr allele is associated with pigmentation of most floral tissues and contains a single copy of the P gene. In contrast, the P-wr allele restricts pigmentation to a subset of floral tissues, and is composed of six gene copies arranged in a tandem head-to-tail array. Each of the six repeats contains a single P gene, including regulatory and coding sequences. Despite the six-fold tandem repetition of P-wr gene copies, P-wr mRNA levels in kernel pericarp are much reduced compared to mRNA levels from the single-copy P-rr gene. Moreover, the P-wr multicopy complex is hypermethylated relative to P-rr. Thus, maize P gene alleles may represent a natural system for studying the effects of methylation and gene copy number on tissue-specific gene expression. We discuss the possibility that somatic pairing of repeated gene copies may be involved in regulating gene expression.
AB - The maize P gene encodes a Myb-homologous transcriptional regulator of flavonoid pigmentation in floral organs, and different P gene alleles condition precise tissue- and organ-specific pigmentation patterns. To determine the molecular basis for allele-specific expression patterns, we have isolated and compared two natural alleles of the P gene which differ in expression, structure and copy number. The P-rr allele is associated with pigmentation of most floral tissues and contains a single copy of the P gene. In contrast, the P-wr allele restricts pigmentation to a subset of floral tissues, and is composed of six gene copies arranged in a tandem head-to-tail array. Each of the six repeats contains a single P gene, including regulatory and coding sequences. Despite the six-fold tandem repetition of P-wr gene copies, P-wr mRNA levels in kernel pericarp are much reduced compared to mRNA levels from the single-copy P-rr gene. Moreover, the P-wr multicopy complex is hypermethylated relative to P-rr. Thus, maize P gene alleles may represent a natural system for studying the effects of methylation and gene copy number on tissue-specific gene expression. We discuss the possibility that somatic pairing of repeated gene copies may be involved in regulating gene expression.
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U2 - 10.1007/s004380050906
DO - 10.1007/s004380050906
M3 - Article
C2 - 9870702
AN - SCOPUS:0031798052
SN - 0026-8925
VL - 260
SP - 372
EP - 380
JO - Molecular and General Genetics
JF - Molecular and General Genetics
IS - 4
ER -