Literature DB >> 1350533

Ten different Polycomb group genes are required for spatial control of the abdA and AbdB homeotic products.

J Simon1, A Chiang, W Bender.   

Abstract

Mutations in genes of the Polycomb (Pc) group cause abnormal segmental development due to ectopic expression of the homeotic products of the Antennapedia and bithorax complexes. Here the requirements for Pc group genes in controlling the abdA and AbdB products of the bithorax complex are described. Embryos containing mutations in the genes Polycomb (Pc), extra sex combs (esc), Enhancer of zeste [E(z)], polyhomeotic (ph), Sex comb on midleg (Scm), Polycomb-like (Pcl), Sex comb extra (Sce), Additional sex combs (Asx), Posterior sex combs (Psc) and pleiohomeotic (pho) were examined. In every case, both abdA and AbdB are expressed outside of their normal domains along the anterior-posterior (A-P) axis, consistent with these Pc group products acting in a single pathway or molecular complex. The earliest detectable ectopic expression is highest in the parasegments immediately adjacent to the normal expression boundary. Surprisingly, in the most severe Pc group mutants, the earliest ectopic AbdB is distributed in a pair-rule pattern. At all stages, ectopic abdA in the epidermis is highest along the anterior edges of the parasegments, in a pattern that mimics the normal abdA cell-specific pattern. These examples of highly patterned mis-expression show that Pc group mutations do not cause indiscriminate activation of homeotic products. We suggest that the ectopic expression patterns result from factors that normally activate abdA and AbdB only in certain parasegments, but that in Pc group mutants these factors gain access to regulatory DNA in all parasegments.

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Year:  1992        PMID: 1350533     DOI: 10.1242/dev.114.2.493

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  125 in total

1.  Site-specific recognition of a 70-base-pair element containing d(GA)(n) repeats mediates bithoraxoid polycomb group response element-dependent silencing.

Authors:  J W Hodgson; B Argiropoulos; H W Brock
Journal:  Mol Cell Biol       Date:  2001-07       Impact factor: 4.272

2.  Establishment of Polycomb silencing requires a transient interaction between PC and ESC.

Authors:  S Poux; R Melfi; V Pirrotta
Journal:  Genes Dev       Date:  2001-10-01       Impact factor: 11.361

3.  Telomeric associated sequences of Drosophila recruit polycomb-group proteins in vivo and can induce pairing-sensitive repression.

Authors:  Antoine Boivin; Christelle Gally; Sophie Netter; Dominique Anxolabéhère; Stéphane Ronsseray
Journal:  Genetics       Date:  2003-05       Impact factor: 4.562

4.  Malignant brain tumor repeats: a three-leaved propeller architecture with ligand/peptide binding pockets.

Authors:  Wooi Koon Wang; Valentina Tereshko; Piernicola Boccuni; Donal MacGrogan; Stephen D Nimer; Dinshaw J Patel
Journal:  Structure       Date:  2003-07       Impact factor: 5.006

5.  A domain shared by the Polycomb group proteins Scm and ph mediates heterotypic and homotypic interactions.

Authors:  A J Peterson; M Kyba; D Bornemann; K Morgan; H W Brock; J Simon
Journal:  Mol Cell Biol       Date:  1997-11       Impact factor: 4.272

6.  Evolutionary conservation and predicted structure of the Drosophila extra sex combs repressor protein.

Authors:  J Ng; R Li; K Morgan; J Simon
Journal:  Mol Cell Biol       Date:  1997-11       Impact factor: 4.272

Review 7.  Role of chromatin states in transcriptional memory.

Authors:  Sharmistha Kundu; Craig L Peterson
Journal:  Biochim Biophys Acta       Date:  2009-02-21

8.  A genetic screen identifies novel polycomb group genes in Drosophila.

Authors:  Andrés Gaytán de Ayala Alonso; Luis Gutiérrez; Cornelia Fritsch; Bernadett Papp; Dirk Beuchle; Jürg Müller
Journal:  Genetics       Date:  2007-08       Impact factor: 4.562

Review 9.  Mediators of reprogramming: transcription factors and transitions through mitosis.

Authors:  Dieter Egli; Garrett Birkhoff; Kevin Eggan
Journal:  Nat Rev Mol Cell Biol       Date:  2008-07       Impact factor: 94.444

10.  Suz12 is essential for mouse development and for EZH2 histone methyltransferase activity.

Authors:  Diego Pasini; Adrian P Bracken; Michael R Jensen; Eros Lazzerini Denchi; Kristian Helin
Journal:  EMBO J       Date:  2004-09-23       Impact factor: 11.598

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