Carles Cristel C, Choffnes-Inada Dan, Reville Keira, Lertpiriyapong Kvin, Fletcher Jennifer C
Plant Gene Expression Center, USDA/UC Berkeley, 800 Buchanan Street, Albany, CA 94710, USA.
Development. 2005 Mar;132(5):897-911. doi: 10.1242/dev.01642. Epub 2005 Jan 26.
The higher-plant shoot apical meristem is a dynamic structure continuously producing cells that become incorporated into new leaves, stems and flowers. The maintenance of a constant flow of cells through the meristem depends on coordination of two antagonistic processes: self-renewal of the stem cell population and initiation of the lateral organs. This coordination is stringently controlled by gene networks that contain both positive and negative components. We have previously defined the ULTRAPETALA1 (ULT1) gene as a key negative regulator of cell accumulation in Arabidopsis shoot and floral meristems, because mutations in ULT1 cause the enlargement of inflorescence and floral meristems, the production of supernumerary flowers and floral organs, and a delay in floral meristem termination. Here, we show that ULT1 negatively regulates the size of the WUSCHEL (WUS)-expressing organizing center in inflorescence meristems. We have cloned the ULT1 gene and find that it encodes a small protein containing a B-box-like motif and a SAND domain, a DNA-binding motif previously reported only in animal transcription factors. ULT1 and its Arabidopsis paralog ULT2 define a novel small gene family in plants. ULT1 and ULT2 are expressed coordinately in embryonic shoot apical meristems, in inflorescence and floral meristems, and in developing stamens, carpels and ovules. Additionally, ULT1 is expressed in vegetative meristems and leaf primordia. ULT2 protein can compensate for mutant ULT1 protein when overexpressed in an ult1 background, indicating that the two genes may regulate a common set of targets during plant development. Downregulation of both ULT genes can lead to shoot apical meristem arrest shortly after germination, revealing a requirement for ULT activity in early development.
高等植物的茎尖分生组织是一种动态结构,不断产生细胞并融入新的叶子、茎和花中。通过分生组织维持恒定的细胞流取决于两个拮抗过程的协调:干细胞群体的自我更新和侧生器官的起始。这种协调受到包含正负成分的基因网络的严格控制。我们之前将 ULTRAPETALA1(ULT1)基因定义为拟南芥茎尖和花分生组织中细胞积累的关键负调控因子,因为 ULT1 基因突变会导致花序和花分生组织增大、产生额外的花和花器官以及花分生组织终止延迟。在这里,我们表明 ULT1 负调控花序分生组织中表达 WUSCHEL(WUS)的组织中心的大小。我们克隆了 ULT1 基因,发现它编码一种含有类 B 盒基序和 SAND 结构域的小蛋白,SAND 结构域是一种以前仅在动物转录因子中报道过的 DNA 结合基序。ULT1 及其拟南芥旁系同源基因 ULT2 在植物中定义了一个新的小基因家族。ULT1 和 ULT2 在胚胎茎尖分生组织、花序和花分生组织以及发育中的雄蕊、心皮和胚珠中协调表达。此外,ULT1 在营养分生组织和叶原基中表达。当在 ult1 背景中过表达时,ULT2 蛋白可以补偿突变的 ULT1 蛋白,这表明这两个基因可能在植物发育过程中调控一组共同的靶标。两个 ULT 基因的下调会导致萌发后不久茎尖分生组织停滞,这揭示了早期发育中对 ULT 活性的需求。