Comparative Transcriptome Profiling of Maize Coleoptilar Nodes during Shoot-Borne Root Initiation

Author:

Muthreich Nils1,Majer Christine1,Beatty Mary2,Paschold Anja3,Schützenmeister André4,Fu Yan5,Malik Waqas Ahmed4,Schnable Patrick S.5,Piepho Hans-Peter4,Sakai Hajime6,Hochholdinger Frank35

Affiliation:

1. Zentrum für Molekularbiologie der Pflanzen, Department of General Genetics, University of Tuebingen, 72076 Tuebingen, Germany (N.M., C.M.)

2. Pioneer Hi-Bred International, Johnston, Iowa 5013 (M.B.)

3. Institute of Crop Science and Resource Conservation, Crop Functional Genomics, University of Bonn, 53113 Bonn, Germany (A.P., F.H.)

4. Institute for Crop Production and Grassland Research, Bioinformatics Unit, University of Hohenheim, 70599 Stuttgart, Germany (A.S., W.A.M., H.-P.P.)

5. Center for Plant Genomics, Iowa State University, Ames, Iowa 50011–3650 (Y.F., P.S.S.); and

6. DuPont Crop Genetics Research, Experimental Station, Wilmington, Delaware 19880–0353 (H.S.)

Abstract

Abstract Maize (Zea mays) develops an extensive shoot-borne root system to secure water and nutrient uptake and to provide anchorage in the soil. In this study, early coleoptilar node (first shoot node) development was subjected to a detailed morphological and histological analysis. Subsequently, microarray profiling via hybridization of oligonucleotide microarrays representing transcripts of 31,355 unique maize genes at three early stages of coleoptilar node development was performed. These pairwise comparisons of wild-type versus mutant rootless concerning crown and seminal roots (rtcs) coleoptilar nodes that do not initiate shoot-borne roots revealed 828 unique transcripts that displayed RTCS-dependent expression. A stage-specific functional analysis revealed overrepresentation of “cell wall,” “stress,” and “development”-related transcripts among the differentially expressed genes. Differential expression of a subset of 15 of 828 genes identified by these microarray experiments was independently confirmed by quantitative real-time-polymerase chain reaction. In silico promoter analyses revealed that 100 differentially expressed genes contained at least one LATERAL ORGAN BOUNDARIES domain (LBD) motif within 1 kb upstream of the ATG start codon. Electrophoretic mobility shift assay experiments demonstrated RTCS binding for four of these promoter sequences, supporting the notion that differentially accumulated genes containing LBD motifs are likely direct downstream targets of RTCS.

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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