4.8 Article

Control of vein network topology by auxin transport

Journal

BMC BIOLOGY
Volume 13, Issue -, Pages -

Publisher

BMC
DOI: 10.1186/s12915-015-0208-3

Keywords

Arabidopsis; Leaf development; Vein network formation; Auxin; PIN genes

Categories

Funding

  1. Discovery Grants of the Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. University of Alberta Doctoral Recruitment Scholarship
  3. NSERC CGS-M Scholarship
  4. NSERC CGS-D Scholarship
  5. 322 Project Scholarship of the Vietnamese Government
  6. University of Alberta-Vietnam International Education Development Scholarship

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Background: Tissue networks such as the vascular networks of plant and animal organs transport signals and nutrients in most multicellular organisms. The transport function of tissue networks depends on topological features such as the number of networks' components and the components' connectedness; yet what controls tissue network topology is largely unknown, partly because of the difficulties in quantifying the effects of genes on tissue network topology. We address this problem for the vein networks of plant leaves by introducing biologically motivated descriptors of vein network topology; we combine these descriptors with cellular imaging and molecular genetic analysis; and we apply this combination of approaches to leaves of Arabidopsis thaliana that lack function of, overexpress or misexpress combinations of four PIN-FORMED (PIN) genes-PIN1, PIN5, PIN6, and PIN8-which encode transporters of the plant signal auxin and are known to control vein network geometry. Results: We find that PIN1 inhibits vein formation and connection, and that PIN6 acts redundantly to PIN1 in these processes; however, the functions of PIN6 in vein formation are nonhomologous to those of PIN1, while the functions of PIN6 in vein connection are homologous to those of PIN1. We further find that PIN8 provides functions redundant and homologous to those of PIN6 in PIN1-dependent inhibition of vein formation, but that PIN8 has no functions in PIN1/PIN6-dependent inhibition of vein connection. Finally, we find that PIN5 promotes vein formation; that all the vein-formation-promoting functions of PIN5 are redundantly inhibited by PIN6 and PIN8; and that these functions of PIN5, PIN6, and PIN8 are independent of PIN1. Conclusions: Our results suggest that PIN-mediated auxin transport controls the formation of veins and their connection into networks.

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