Bif2 barren inflorescence2 explained

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Function. Regulation of auxin transport during axillary Meristem and lateral organ initiation.

Summary[1] The bif2 mutation affects all axillary meristems in the plant. The tassel has fewer branches, spikelets, florets and floral organs (McSteen and Hake 2001).[2] The ear shoot, if it forms, has very few kernels. The mutant plants also have defects in vegetative development as they make fewer tillers (in a tb1 mutant background) and make one or two fewer leaves than normal. The bif2 gene encodes a serine threonine protein kinase (McSteen et al 2007)[3] that phosphorylates auxin efflux carrier ZmPIN1a (Skirpan et al 2008)[4] and BHLH transcription factor BARREN STALK1 (Skirpan et al 2008). Natural variation in bif2 alleles are associated with tassel branch number and plant height (Pressoir et al 2009).[5]

First report. Briggs and Johal 1992[6]

Chromosome Location Based on B-A chromosomal translocation data and tight linkage to the RFLP marker umc67a (McSteen and Hake 2001) and the 2010 B73_v2 maize reference genome sequence assembly.[7] Genetically mapped SNPs near the gene include rs131816257, rs131816315, and rs131816316.

Phenotypes Mutations in the gene produce plants where tassels, or male inflorescences have fewer branches, spikelets, florets and floral organs. The ear shoot or female inflorescence, if it forms, has very few kernels. Natural variations of the bif2 gene have been found to affect tassel branch number and plant height (Pressoir et al 2009)

Gene Product Serine/threonine protein kinase that phosphorylates the PIN1a (Skirpan et al 2009)[8] and BA2 proteins in vitro.

LINKS

Notes and References

  1. McSteen. P. Paula McSteen. maize gene review bif2. Maize Genetics Cooperation Newsletter. 2013. 86. 37.
  2. McSteen. P. Paula McSteen. Hake, S. barren inflorescence2 regulates axillary meristem development in the maize inflorescence.. Development. Aug 2001. 128. 15. 2881–91. 10.1242/dev.128.15.2881. 11532912.
  3. McSteen. P. Paula McSteen. Malcomber, S . Skirpan, A . Lunde, C . Wu, X . Kellogg, E . Hake, S . barren inflorescence2 Encodes a co-ortholog of the PINOID serine/threonine kinase and is required for organogenesis during inflorescence and vegetative development in maize.. Plant Physiology. Jun 2007. 144. 2. 1000–11. 17449648. 10.1104/pp.107.098558. 1914211.
  4. Skirpan. A. Wu, X . McSteen, P . Genetic and physical interaction suggest that BARREN STALK 1 is a target of BARREN INFLORESCENCE2 in maize inflorescence development.. The Plant Journal. Sep 2008. 55. 5. 787–97. 18466309. 10.1111/j.1365-313X.2008.03546.x.
  5. Pressoir. G. Brown, PJ . Zhu, W . Upadyayula, N . Rocheford, T . Buckler, ES . Kresovich, S . Natural variation in maize architecture is mediated by allelic differences at the PINOID co-ortholog barren inflorescence2.. The Plant Journal. May 2009. 58. 4. 618–28. 19154226. 10.1111/j.1365-313X.2009.03802.x. free.
  6. Briggs. SP. Johal G. A recessive barren-inflorescence mutation. Maize Genetics Cooperation Newsletter. 1992. 66. 51. 21 November 2013.
  7. Schnable. PS . etal . The B73 maize genome: complexity, diversity, and dynamics.. Science. Nov 20, 2009. 326. 5956. 1112–5. 19965430. 10.1126/science.1178534 . 2009Sci...326.1112S . 21433160 .
  8. Skirpan. A. Culler, AH . Gallavotti, A . Jackson, D . Cohen, JD . McSteen, P . BARREN INFLORESCENCE2 interaction with ZmPIN1a suggests a role in auxin transport during maize inflorescence development.. Plant & Cell Physiology. Mar 2009. 50. 3. 652–7. 19153156. 10.1093/pcp/pcp006. free.