The role of binding site cluster strength in Bicoid-dependent patterning in Drosophila.

The maternal morphogen Bicoid (Bcd) is distributed in an embryonic gradient that is critical for patterning the anterior-posterior (AP) body plan in Drosophila. Previous work identified several target genes that respond directly to Bcd-dependent activation. Positioning of these targets along the AP axis is thought to be controlled by cis-regulatory modules (CRMs) that contain clusters of Bcd-binding sites of different "strengths." Here we use a combination of Bcd-site cluster analysis and evolutionary conservation to predict Bcd-dependent CRMs. We tested 14 predicted CRMs by in vivo reporter gene assays; 11 show Bcd-dependent activation, which brings the total number of known Bcd target elements to 21. Some CRMs drive expression patterns that are restricted to the most anterior part of the embryo, whereas others extend into middle and posterior regions. However, we do not detect a strong correlation between AP position of target gene expression and the strength of Bcd site clusters alone. Rather, we find that binding sites for other activators, including Hunchback and Caudal correlate with CRM expression in middle and posterior body regions. Also, many Bcd-dependent CRMs contain clusters of sites for the gap protein Kruppel, which may limit the posterior extent of activation by the Bcd gradient. We propose that the key design principle in AP patterning is the differential integration of positive and negative transcriptional information at the level of individual CRMs for each target gene.

[1]  R. Lehmann,et al.  hunchback, a gene required for segmentation of an anterior and posterior region of the Drosophila embryo. , 1987, Developmental biology.

[2]  Marek Mlodzik,et al.  Expression of the caudal gene in the germ line of Drosophila: Formation of an RNA and protein gradient during early embryogenesis , 1987, Cell.

[3]  D Bopp,et al.  The role of localization of bicoid RNA in organizing the anterior pattern of the Drosophila embryo. , 1988, The EMBO journal.

[4]  M. Bate,et al.  The development of Drosophila melanogaster , 1993 .

[5]  J. Fak,et al.  Transcriptional Control in the Segmentation Gene Network of Drosophila , 2004, PLoS biology.

[6]  J. Nambu,et al.  The Drosophila fish-hook gene encodes a HMG domain protein essential for segmentation and CNS development. , 1996, Development.

[7]  H. Jäckle,et al.  Mechanism and Bicoid‐dependent control of hairy stripe 7 expression in the posterior region of the Drosophila embryo , 1997, The EMBO journal.

[8]  S. Carroll,et al.  Positioning adjacent pair-rule stripes in the posterior Drosophila embryo. , 1994, Development.

[9]  Dmitri Papatsenko,et al.  A self-organizing system of repressor gradients establishes segmental complexity in Drosophila , 2003, Nature.

[10]  T. Tuschl,et al.  Identification of Novel Genes Coding for Small Expressed RNAs , 2001, Science.

[11]  Wolfgang Driever,et al.  The bicoid protein is a positive regulator of hunchback transcription in the early Drosophila embryo , 1989, Nature.

[12]  W. Gehring,et al.  The Drosophila sloppy paired locus encodes two proteins involved in segmentation that show homology to mammalian transcription factors. , 1992, Genes & development.

[13]  C. Desplan,et al.  Bicoid-independent formation of thoracic segments in Drosophila. , 2000, Science.

[14]  C. Nüsslein-Volhard,et al.  The bicoid protein determines position in the Drosophila embryo in a concentration-dependent manner , 1988, Cell.

[15]  Daniel St Johnston,et al.  Seeing Is Believing The Bicoid Morphogen Gradient Matures , 2004, Cell.

[16]  Dmitri Papatsenko,et al.  Quantitative analysis of binding motifs mediating diverse spatial readouts of the Dorsal gradient in the Drosophila embryo. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Claude Desplan,et al.  Synergy between the hunchback and bicoid morphogens is required for anterior patterning in Drosophila , 1994, Cell.

[18]  P. Lawrence,et al.  Borders of parasegments in Drosophila embryos are delimited by the fushi tarazu and even-skipped genes , 1987, Nature.

[19]  Anna G. Nazina,et al.  Homotypic regulatory clusters in Drosophila. , 2003, Genome research.

[20]  S. Small In vivo analysis of lacZ fusion genes in transgenic Drosophila melanogaster. , 2000, Methods in enzymology.

[21]  R. Schuh,et al.  Regulation of Drosophila spalt gene expression , 1997, Mechanisms of Development.

[22]  V. Pirrotta,et al.  A novel spatial transcription pattern associated with the segmentation gene, giant, of Drosophila. , 1989, The EMBO journal.

[23]  Danyang Yu,et al.  Groucho-dependent repression by sloppy-paired 1 differentially positions anterior pair-rule stripes in the Drosophila embryo. , 2004, Developmental biology.

[24]  Anna G. Nazina,et al.  Extraction of functional binding sites from unique regulatory regions: the Drosophila early developmental enhancers. , 2002, Genome research.

[25]  C. Nüsslein-Volhard,et al.  Organization of anterior pattern in the Drosophila embryo by the maternal gene bicoid , 1986, Nature.

[26]  H. Jäckle,et al.  Trans- and cis-acting requirements for blastodermal expression of the head gap gene buttonhead , 1995, Mechanisms of Development.

[27]  Lei Wang,et al.  bowel, an odd‐skipped homolog, functions in the terminal pathway during Drosophila embryogenesis. , 1996, The EMBO journal.

[28]  G. Struhl,et al.  Decoding positional information: regulation of the pair-rule gene hairy. , 1990, Development.

[29]  M. Frasch,et al.  Survey of forkhead domain encoding genes in the Drosophila genome: Classification and embryonic expression patterns , 2004, Developmental dynamics : an official publication of the American Association of Anatomists.

[30]  C. Nüsslein-Volhard,et al.  A gradient of bicoid protein in Drosophila embryos , 1988, Cell.

[31]  Wolfgang Driever,et al.  Determination of spatial domains of zygotic gene expression in the Drosophila embryo by the affinity of binding sites for the bicoid morphogen , 1989, Nature.

[32]  Diethard Tautz,et al.  Finger protein of novel structure encoded by hunchback, a second member of the gap class of Drosophila segmentation genes , 1987, Nature.

[33]  L. Pachter,et al.  Strategies and tools for whole-genome alignments. , 2002, Genome research.

[34]  M. Noll,et al.  Isolation of the paired gene of Drosophila and its spatial expression during early embryogenesis , 1986, Nature.

[35]  S. Small,et al.  Two distinct mechanisms for differential positioning of gene expression borders involving the Drosophila gap protein giant. , 1998, Development.

[36]  K. Struhl,et al.  The gradient morphogen bicoid is a concentration-dependent transcriptional activator , 1989, Cell.

[37]  Norbert Perrimon,et al.  The orthodenticle gene is regulated by bicoid and torso and specifies Drosophila head development , 1990, Nature.

[38]  S. Leibler,et al.  Establishment of developmental precision and proportions in the early Drosophila embryo , 2002, Nature.

[39]  M. Levine,et al.  Regulation of even‐skipped stripe 2 in the Drosophila embryo. , 1992, The EMBO journal.

[40]  A. Goriely,et al.  A functional homologue of goosecoid in Drosophila. , 1996, Development.

[41]  S. Small,et al.  Anterior repression of a Drosophila stripe enhancer requires three position-specific mechanisms. , 2002, Development.

[42]  M Hoch,et al.  cis‐acting control elements for Krüppel expression in the Drosophila embryo. , 1990, The EMBO journal.

[43]  G. Rubin,et al.  Genetic transformation of Drosophila with transposable element vectors. , 1982, Science.

[44]  Norbert Perrimon,et al.  Activation of posterior gap gene expression in the Drosophila blastoderm , 1995, Nature.

[45]  W. Gehring,et al.  Three maternal coordinate systems cooperate in the patterning of the Drosophila head. , 1994, Development.

[46]  Q Gao,et al.  Targeting gene expression to the head: the Drosophila orthodenticle gene is a direct target of the Bicoid morphogen. , 1998, Development.

[47]  Robert J. Diaz,et al.  The Drosophila gene tailless is expressed at the embryonic termini and is a member of the steroid receptor superfamily , 1990, Cell.

[48]  M. Fujioka,et al.  Analysis of an even-skipped rescue transgene reveals both composite and discrete neuronal and early blastoderm enhancers, and multi-stripe positioning by gap gene repressor gradients. , 1999, Development.

[49]  M. Ashburner,et al.  The Dichaete gene of Drosophila melanogaster encodes a SOX-domain protein required for embryonic segmentation. , 1996, Development.