The Maize MID-COMPLEMENTING ACTIVITY Homolog CELL NUMBER REGULATOR13/NARROW ODD DWARF Coordinates Organ Growth and Tissue Patterning[OPEN]
The Maize MID-COMPLEMENTING ACTIVITY Homolog CELL NUMBER REGULATOR13/NARROW ODD DWARF Coordinates Organ Growth and Tissue Patterning[OPEN]
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玉米中补体活性同源细胞数调节器13/窄奇矮矮化协调器官生长和组织模式[打开]
DOI:
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发表时间:
2017
期刊:
影响因子:
--
通讯作者:
S. Hake
中科院分区:
文献类型:
--
作者:
Marisa Rosa;M. Abraham;M. Lewis;J. P. Fonseca;Wang Tian;Vicente Ramírez;S. Luan;M. Pauly;S. Hake
Phenotypic and transcriptome analysis indicate that NARROW ODD DWARF, the MID-COMPLEMENTING ACTIVITY homolog, regulates organ growth, tissue patterning, and pathogen responses in maize. Organogenesis occurs through cell division, expansion, and differentiation. How these cellular processes are coordinated remains elusive. The maize (Zea mays) leaf provides a robust system to study cellular differentiation due to its distinct tissues and cell types. The narrow odd dwarf (nod) mutant displays defects at both the cellular and tissue level that increase in severity throughout growth. nod mutant leaves have reduced size due to fewer and smaller cells compared with the wild type. The juvenile-to-adult transition is delayed, and proximal distal-patterning is abnormal in this mutant. Differentiation of specialized cells such as those forming stomata and trichomes is incomplete. Analysis of nod-1 sectors suggests that NOD plays a cell-autonomous function in the leaf. We cloned nod positionally and found that it encodes CELL NUMBER REGULATOR13 (CNR13), the maize MID-COMPLEMENTING ACTIVITY homolog. CNR13/NOD is localized to the membrane and is enriched in dividing tissues. Transcriptome analysis of nod mutants revealed overrepresentation of cell wall, hormone metabolism, and defense gene categories. We propose that NOD coordinates cell activity in response to intrinsic and extrinsic cues.
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DOI:
10.1083/jcb.152.1.231
发表时间:
2001-01-08
期刊:
The Journal of cell biology
影响因子:
--
作者:
Smith LG;Gerttula SM;Han S;Levy J
通讯作者:
Levy J
影响因子:
3.3
作者:
Eric M. Muller;Emily G. Locke;Kyle W. Cunningham
通讯作者:
Eric M. Muller;Emily G. Locke;Kyle W. Cunningham
影响因子:
7.2
作者:
Earley, KW;Haag, JR;Pikaard, CS
通讯作者:
Pikaard, CS
影响因子:
10.5
作者:
Moreno, MA;Harper, LC;Freeling, M
通讯作者:
Freeling, M
影响因子:
4.8
作者:
Khan, Mamoona;Rozhon, Wilfried;Poppenberger, Brigitte
通讯作者:
Poppenberger, Brigitte