» Articles » PMID: 22902700

A Crosstalk of Auxin and GA During Tuber Development

Overview
Specialty Biology
Date 2012 Aug 21
PMID 22902700
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

Several hormones have been studied for their effect on tuber initiation and development. Until recently, the hormone with the most prominent role in tuber initiation was attributed to GA. Genes involved in GA degradation do exhibit an upregulated profile during early stages of tuber development, leading to a rapid decrease of active GA content, thereby facilitating stolon-tip swelling. While GA is known to be involved in shoot and stolon elongation, the development of the new tuberorgan requires changes in meristem identity and the reorientation ofthe plane of cell division. In other developmental processes, such as embryo patterning, flower development and lateral root initiation auxin plays a key role. Recent evidence on the involvement of auxin in tuber formation was providedby the measurement of auxin content in swelling stolons. Auxin content in the stolon tips increased several fold prior to tuber swelling. In vitro tuberisation experiments with auxin applications support the role of auxin during tuber initiation. Taken together, it is becoming clear that the initiation and induction of tubers in potato is a developmental process that appears to be regulated by a crosstalk between GA and auxin.

Citing Articles

Regulation of storage organ formation by long-distance tuberigen signals in potato.

Bao X, Zhu Y, Li G, Liu L Hortic Res. 2025; 12(4):uhae360.

PMID: 40070401 PMC: 11894528. DOI: 10.1093/hr/uhae360.


Transcriptome Analysis Reveals Novel Genes Potentially Involved in Tuberization in Potato.

Zhang M, Jian H, Shang L, Wang K, Wen S, Li Z Plants (Basel). 2024; 13(6).

PMID: 38592791 PMC: 10975680. DOI: 10.3390/plants13060795.


Hormones and carbohydrates synergistically regulate the formation of swollen roots in a Chinese cabbage translocation line.

Ren X, Ma W, Xuan S, Li D, Wang Y, Xu Y Hortic Res. 2023; 10(8):uhad121.

PMID: 37554342 PMC: 10405133. DOI: 10.1093/hr/uhad121.


Dynamic transcriptome profiling provides insights into rhizome enlargement in ginger (Zingiber officinale Rosc.).

Ren Y, Li W, Li Z, Zhang W, Jue D, Xing H PLoS One. 2023; 18(7):e0287969.

PMID: 37450442 PMC: 10348538. DOI: 10.1371/journal.pone.0287969.


Research progress on the bulb expansion and starch enrichment in taro .

Zhang E, Shen W, Jiang W, Li W, Wan X, Yu X PeerJ. 2023; 11:e15400.

PMID: 37309370 PMC: 10257899. DOI: 10.7717/peerj.15400.


References
1.
Bou-Torrent J, Martinez-Garcia J, Garcia-Martinez J, Prat S . Gibberellin A1 metabolism contributes to the control of photoperiod-mediated tuberization in potato. PLoS One. 2011; 6(9):e24458. PMC: 3178525. DOI: 10.1371/journal.pone.0024458. View

2.
Ishida S, Takahashi Y, Nagata T . Isolation of cDNA of an auxin-regulated gene encoding a G protein beta subunit-like protein from tobacco BY-2 cells. Proc Natl Acad Sci U S A. 1993; 90(23):11152-6. PMC: 47940. DOI: 10.1073/pnas.90.23.11152. View

3.
Taoka K, Ohki I, Tsuji H, Furuita K, Hayashi K, Yanase T . 14-3-3 proteins act as intracellular receptors for rice Hd3a florigen. Nature. 2011; 476(7360):332-5. DOI: 10.1038/nature10272. View

4.
Faivre-Rampant O, Cardle L, Marshall D, Viola R, Taylor M . Changes in gene expression during meristem activation processes in Solanum tuberosum with a focus on the regulation of an auxin response factor gene. J Exp Bot. 2004; 55(397):613-22. DOI: 10.1093/jxb/erh075. View

5.
Dhonukshe P, Weits D, Cruz-Ramirez A, Deinum E, Tindemans S, Kakar K . A PLETHORA-auxin transcription module controls cell division plane rotation through MAP65 and CLASP. Cell. 2012; 149(2):383-96. DOI: 10.1016/j.cell.2012.02.051. View