Zhang Feng, Peterson Thomas
Department of Genetics, Development, and Cell Biology, Iowa State University, Ames, Iowa 50010, USA.
Plant Cell. 2005 Mar;17(3):903-14. doi: 10.1105/tpc.104.029660. Epub 2005 Feb 18.
The maize (Zea mays) p1 (for pericarp color1) gene encodes an R2R3 Myb-like transcription factor that regulates the flavonoid biosynthetic pathway in floral organs, most notably kernel pericarp and cob. Alleles of the p1 gene condition distinct tissue-specific pigmentation patterns; to elucidate the molecular basis of these allele-specific expression patterns, we characterized two novel P1-rw (for red pericarp/white cob) alleles, P1-rw1077 and P1-rw751Ac. Structural analysis of P1-rw1077 indicated that this allele was generated by recombination between p1 and the tightly linked paralogous gene, p2. In the resulting gene, the p1 coding sequence was replaced by the p2 coding sequence, whereas the flanking p1 regulatory sequences remained largely preserved. The red pericarp color specified by P1-rw1077 suggests that the p1- and p2-encoded proteins are functionally equivalent as regulatory factors in the flavonoid biosynthesis pathway. Sequence analysis shows that the P1-rw1077 allele lacks a 386-bp sequence in a distal enhancer region 5 kb upstream of the transcription start site. An independently derived P1-rw allele contains an Ac insertion into the same sequence, indicating that this site likely contains cob glume-specific regulatory elements.
玉米(Zea mays)的p1(果皮颜色1)基因编码一种R2R3类Myb转录因子,该因子调控花器官中的类黄酮生物合成途径,最显著的是在籽粒果皮和雌穗轴中。p1基因的等位基因决定了不同的组织特异性色素沉着模式;为了阐明这些等位基因特异性表达模式的分子基础,我们鉴定了两个新的P1-rw(红色果皮/白色雌穗轴)等位基因,P1-rw1077和P1-rw751Ac。对P1-rw1077的结构分析表明,该等位基因是由p1与紧密连锁的旁系同源基因p2之间的重组产生的。在产生的基因中,p1编码序列被p2编码序列取代,而侧翼的p1调控序列基本保留。P1-rw1077所决定的红色果皮颜色表明,p1和p2编码的蛋白质在类黄酮生物合成途径中作为调控因子在功能上是等效的。序列分析表明,P1-rw1077等位基因在转录起始位点上游5 kb的远端增强子区域缺少一个386 bp的序列。一个独立衍生的P1-rw等位基因在同一序列中插入了一个Ac,表明该位点可能包含雌穗轴颖片特异性调控元件。