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Using NASA's GeneLab for VESGEN Systems Analysis of Vascular Phenotypes from Stress and Other Signaling PathwaysOne fundamental requirement shared by humans with all higher terrestrial life forms, including other vertebrates, insects, and higher land plants, is a complex, fractally branching vascular system. NASA's VESsel GENeration Analysis (VESGEN) software maps and quantifies vascular trees, networks, and tree-network composites according to weighted physiological rules such as vessel connectivity, tapering and bifurcational branching. According to fluid dynamics, successful vascular transport requires a complex distributed system of highly regulated laminar flow. Microvascular branching rules within vertebrates, dicot leaves and the other organisms therefore display many similarities. A unifying perspective is that vascular patterning offers a useful readout of molecular signaling that necessarily integrates these complex pathways. VESGEN has elucidated changes in vascular pattern resulting from inflammatory, developmental and other signaling within numerous tissues and major model organisms studied for Space Biology. For a new VESGEN systems approach, we analyzed differential gene expression in leaves of Arabidopsis thaliana reported by GeneLab (GLDS-7) for spaceflight. Vascularrelated changes in leaf gene expression were identified that can potentially be phenocopied by mutants in ground-based experiments. To link transcriptional, protein and other molecular change with phenotype, alterations in the spatial and dynamic dimensions of vascular patterns for Arabidopsis leaves and other model species are being co-localized with signaling patterns of single molecular expression analyzed as information dimensions. Previously, Drosophila microarray data returned from space suggested significant changes in genes related to wing venation development that include EGF, Notch, Hedghog, Wingless and Dpp signaling. Phenotypes of increasingly abnormal ectopic wing venation in the (non-spaceflight) Drosophila wing generated by overexpression of a Notch antagonist were analyzed by VESGEN. Other VESGEN research applications include the mouse retina, GI and coronary vessels, avian placental analogs and translational studies in the astronaut retina related to health challenges for long-duration missions.
Document ID
20160014685
Acquisition Source
Ames Research Center
Document Type
Presentation
Authors
Parsons-Wingerter, P.
(NASA Ames Research Center Moffett Field, CA United States)
Weitzel, Alexander
(Grand Valley State Univ. Allendale, MI, United States)
Vyas, R. J.
(SGT, Inc. Moffett Field, CA, United States)
Murray, M. C.
(Blue Marble Space Seattle, WA, United States)
Vickerman, M. B.
(Ohio Univ. Athens, OH, United States)
Bhattacharya, S.
(NASA Ames Research Center Moffett Field, CA United States)
Wyatt, S. E.
(Ohio Univ. Athens, OH, United States)
Date Acquired
December 19, 2016
Publication Date
October 26, 2016
Subject Category
Life Sciences (General)
Exobiology
Report/Patent Number
ARC-E-DAA-TN36569
Meeting Information
Meeting: American Society for Gravity and Space Research (ASGSR) Conference 2016
Location: Cleveland, OH
Country: United States
Start Date: October 26, 2016
End Date: October 29, 2016
Sponsors: American Society for Gravitational and Space Research
Funding Number(s)
CONTRACT_GRANT: NNX15AG98A
CONTRACT_GRANT: NNA14AA60C
Distribution Limits
Public
Copyright
Public Use Permitted.
Keywords
Venation
system biology
VESGEN
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