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PHB  -  homeobox-leucine zipper protein ATHB-14

Arabidopsis thaliana

Synonyms: ARABIDOPSIS THALIANA HOMEOBOX PROTEIN 14, ATHB-14, ATHB14, PHABULOSA, PHABULOSA 1D, ...
 
 
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High impact information on PHB

  • Role of PHABULOSA and PHAVOLUTA in determining radial patterning in shoots [1].
  • We propose that the initial asymmetric leaf development is regulated primarily by mutual antagonism between KANADI and PHB-like genes, which is translated into polar YABBY expression [2].
  • Simultaneous loss-of-function of PHABULOSA, PHAVOLUTA, and REVOLUTA abaxializes cotyledons, abolishes the formation of the primary apical meristem, and in severe cases, eliminates bilateral symmetry; these phenotypes implicate these three genes in radial patterning of both embryonic and postembryonic growth [3].
  • In Arabidopsis, gain-of-function alleles of PHAVOLUTA and PHABULOSA, members of the class III HD-ZIP gene family, result in adaxialization of lateral organs [3].
  • Thus, both WUS and PHB affect processes downstream of NZZ action during the transition from proximal--distal to adaxial--abaxial ovule development [4].
 

Biological context of PHB

  • Low levels of methylation are detected in wt PHB DNA isolated from undifferentiated tissues [5].
  • Here we show that the zinc-finger protein SERRATE acts in a microRNA (miRNA) gene-silencing pathway to regulate expression of the HD-Zip III gene PHABULOSA (PHB) while also limiting the competence of shoot tissue to respond to KNOX expression [6].
 

Regulatory relationships of PHB

  • The alterations in polarity establishment are associated with expansion in the expression domain of the PHB-like genes and reduction in the expression of the previously described abaxial-promoting YABBY genes [7].
 

Other interactions of PHB

  • We found that NZZ is required to restrict PHB expression to the distal chalaza, from where the inner integument initiates [4].
  • PHB expression is not established in the distal chalaza of two mutants, aintegumenta (ant) and wus, which fail to form integuments [4].
  • Furthermore, we examined the expression pattern of PHB, INO, and WUS in ovules of plants, which are affected in integument initiation and thus defective in the transition from proximal-distal to adaxial-abaxial development [4].

References

  1. Role of PHABULOSA and PHAVOLUTA in determining radial patterning in shoots. McConnell, J.R., Emery, J., Eshed, Y., Bao, N., Bowman, J., Barton, M.K. Nature (2001) [Pubmed]
  2. Asymmetric leaf development and blade expansion in Arabidopsis are mediated by KANADI and YABBY activities. Eshed, Y., Izhaki, A., Baum, S.F., Floyd, S.K., Bowman, J.L. Development (2004) [Pubmed]
  3. Radial patterning of Arabidopsis shoots by class III HD-ZIP and KANADI genes. Emery, J.F., Floyd, S.K., Alvarez, J., Eshed, Y., Hawker, N.P., Izhaki, A., Baum, S.F., Bowman, J.L. Curr. Biol. (2003) [Pubmed]
  4. Pattern formation during early ovule development in Arabidopsis thaliana. Sieber, P., Gheyselinck, J., Gross-Hardt, R., Laux, T., Grossniklaus, U., Schneitz, K. Dev. Biol. (2004) [Pubmed]
  5. MicroRNA binding sites in Arabidopsis class III HD-ZIP mRNAs are required for methylation of the template chromosome. Bao, N., Lye, K.W., Barton, M.K. Dev. Cell (2004) [Pubmed]
  6. SERRATE coordinates shoot meristem function and leaf axial patterning in Arabidopsis. Grigg, S.P., Canales, C., Hay, A., Tsiantis, M. Nature (2005) [Pubmed]
  7. Establishment of polarity in lateral organs of plants. Eshed, Y., Baum, S.F., Perea, J.V., Bowman, J.L. Curr. Biol. (2001) [Pubmed]
 
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