POSTTRANSCRIPTIONAL REGULATION OF A SALT-INDUCIBLE ALFALFA GENE ENCODING A PUTATIVE CHIMERIC PROLINE-RICH CELL-WALL PROTEIN

被引:92
作者
DEUTCH, CE
WINICOV, I
机构
[1] UNIV NEVADA, DEPT BIOCHEM, RENO, NV 89557 USA
[2] UNIV NEVADA, DEPT MICROBIOL, RENO, NV 89557 USA
[3] UNIV NEVADA, DEPT BIOL SCI, LAS VEGAS, NV 89154 USA
关键词
ALFALFA; CELL WALL PROTEIN; CYSTEINE-RICH DOMAIN; PROLINE-RICH PROTEIN; MESSENGER-RNA STABILITY; SALT-REGULATED GENES;
D O I
10.1007/BF00020194
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
A cDNA previously shown to identify a salt-inducible root-specific transcript in Medicago saliva was used to screen an alfalfa library for the corresponding genomic sequence. One positive clone was recovered. The nucleotide sequence of a subclone contained a 329 bp 5' region upstream of the first ATG codon, a 1143 bp coding segment, and a 447 bp 3'-untranslated region interrupted by a single 475 bp intron. Translation of the coding segment, which was designated MsPRP2, suggested it encodes a chimeric 40569 Da cell wall protein with an amino-terminal signal sequence, a repetitive proline-rich sequence, and a cysteine-rich carboxyl-terminal sequence homologous to nonspecific lipid transfer proteins. The 3'-untranslated region of MsPRP2 contained a sequence similar to one found to destabilize mRNAs transcribed from the elicitor-regulated proline-rich protein gene PvPRP1. Transcription run-on experiments using nuclei from salt-sensitive and salt-tolerant alfalfa callus suggested that the accumulation of MsPRP2 transcripts in salt-tolerant alfalfa cells grown in the presence of salt is due primarly to increased mRNA stability. The MsPRP2 gene thus may be a useful model for studying post-transcriptional salt-regulated expression of cell wall proteins.
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页码:411 / 418
页数:8
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