scholarly journals Fusion of the additional sex combs like 1 and teashirt zinc finger homeobox 2 genes resulting from ider(20q) aberration in a patient with myelodysplastic syndrome

2013 ◽  
Vol 164 (1) ◽  
pp. 153-155 ◽  
Author(s):  
Jana Brezinova ◽  
Iveta Sarova ◽  
Halka Buryova ◽  
Jana Markova ◽  
Sarka Ransdorfova ◽  
...  
Keyword(s):  
Myelodysplastic Syndrome ◽  
Zinc Finger ◽  
Sex Combs ◽  
Additional Sex Combs

Comparison of germline mosaics of genes in the Polycomb group of Drosophila melanogaster.

Genetics ◽  
1995 ◽  
Vol 140 (1) ◽  
pp. 231-243 ◽  
Author(s):  
M C Soto ◽  
T B Chou ◽  
W Bender
Keyword(s):  
Drosophila Melanogaster ◽  
Target Genes ◽  
Cell Types ◽  
Mitotic Recombination ◽  
Polycomb Group ◽  
Specific Cell ◽  
Independent Functions ◽  
Sex Combs ◽  
Null Phenotype ◽  
Additional Sex Combs

Abstract The genes of the Polycomb group (PcG) repress the genes of the bithorax and Antennapedia complexes, among others. To observe a null phenotype for a PcG gene, one must remove its maternal as well as zygotic contribution to the embryo. Five members of the PcG group are compared here: Enhancer of Polycomb [E(Pc)], Additional sex combs (Asx), Posterior sex combs (Psc), Suppressor of zeste 2 [Su (z) 2] and Polycomblike (Pcl). The yeast recombinase (FLP) system was used to induce mitotic recombination in the maternal germline. Mutant embryos were analyzed by staining with antibodies against six target genes of the PcG. The loss of the maternal component leads to enhanced homeotic phenotypes and to unique patterns of misexpression. E(Pc) and Su(z) 2 mutations had only subtle effects on the target genes, even when the maternal contributions were removed. Asx and Pcl mutants show derepression of the targets only in specific cell types. Psc shows unusual effects on two of the targets, Ultrabithorax and abdominal-A. These results show that the PcG genes do not act only in a common complex or pathway; they must have some independent functions.

The Additional sex combs gene of Drosophila encodes a chromatin protein that binds to shared and unique Polycomb group sites on polytene chromosomes

Development ◽  
1998 ◽  
Vol 125 (7) ◽  
pp. 1207-1216 ◽  
Author(s):  
D.A. Sinclair ◽  
T.A. Milne ◽  
J.W. Hodgson ◽  
J. Shellard ◽  
C.A. Salinas ◽  
...  
Keyword(s):  
Target Genes ◽  
Position Effect ◽  
Polytene Chromosomes ◽  
Polycomb Group ◽  
Position Effect Variegation ◽  
Sex Combs ◽  
Effect Variegation ◽  
The Central Nervous System ◽  
Additional Sex Combs ◽  
Site Recognition

The Additional sex combs (Asx) gene of Drosophila is a member of the Polycomb group of genes, which are required for maintenance of stable repression of homeotic and other loci. Asx is unusual among the Polycomb group because: (1) one Asx allele exhibits both anterior and posterior transformations; (2) Asx mutations enhance anterior transformations of trx mutations; (3) Asx mutations exhibit segmentation phenotypes in addition to homeotic phenotypes; (4) Asx is an Enhancer of position-effect variegation and (5) Asx displays tissue-specific derepression of target genes. Asx was cloned by transposon tagging and encodes a protein of 1668 amino acids containing an unusual cysteine cluster at the carboxy terminus. The protein is ubiquitously expressed during development. We show that Asx is required in the central nervous system to regulate Ultrabithorax. ASX binds to multiple sites on polytene chromosomes, 70% of which overlap those of Polycomb, polyhomeotic and Polycomblike, and 30% of which are unique. The differences in target site recognition may account for some of the differences in Asx phenotypes relative to other members of the Polycomb group.

scholarly journals The Role of Additional Sex Combs-Like Proteins in Cancer

2016 ◽  
Vol 6 (10) ◽  
pp. a026526 ◽  
Author(s):  
Jean-Baptiste Micol ◽  
Omar Abdel-Wahab
Keyword(s):  
Sex Combs ◽  
Additional Sex Combs

scholarly journals A de novo Variant of ASXL1 Is Associated With an Atypical Phenotype of Bohring-Opitz Syndrome: Case Report and Literature Review

2021 ◽  
Vol 9 ◽  
Author(s):  
Weiqing Zhao ◽  
Xiao Hu ◽  
Ye Liu ◽  
Xike Wang ◽  
Yun Chen ◽  
...  
Keyword(s):  
De Novo ◽  
Global Developmental Delay ◽  
Heterozygous Mutation ◽  
Nasal Bridge ◽  
Sex Combs ◽  
Subarachnoid Spaces ◽  
Opitz Syndrome ◽  
Additional Sex Combs ◽  
Atypical Phenotype ◽  
De Novo Variant

Bohring-Opitz syndrome (BOS) is a rare genetic disease first reported by Bohring et al. in 1999. With the recent development of exome sequencing (ES), de novo truncating mutations in the additional sex-combs-like 1 (ASXL1) gene have been causally implicated in BOS. Herein, we describe a 7-month-old girl with intrauterine growth restriction, severe pulmonary infection, seizures, and craniofacial abnormalities (microcephaly, micro/retrognathia, hypertelorism, depressed nasal bridge, low-set ears and hypertrichosis) at birth. At a later stage, the patient developed global developmental delay. We performed ES and identified a de novo heterozygous mutation in ASXL1, namely, c.1210C>T/p.R404*. However, this case did not have trigonocephaly, facial hemangioma, prominent eyes, myopia, BOS posture, or brain abnormalities (enlarged subarachnoid spaces, agenesis of the corpus callosum, moderately enlarged cerebral ventricles, or prominent frontal subarachnoid spaces), which are common characteristics in most patients with BOS-harboring ASXL1 mutations. These new data expand the phenotype of BOS driven by ASXL1 and may assist in more accurately delineating the phenotypes caused by variants of this gene.

Additional sex combs-likefamily genes are required for normal cardiovascular development

genesis ◽  
2014 ◽  
Vol 52 (7) ◽  
pp. 671-686 ◽  
Author(s):  
Andrea L. McGinley ◽  
Yanyang Li ◽  
Zane Deliu ◽  
Q. Tian Wang
Keyword(s):  
Cardiovascular Development ◽  
Sex Combs ◽  
Additional Sex Combs

scholarly journals HHEX promotes myeloid transformation in cooperation with mutant ASXL1

Blood ◽  
2020 ◽  
Author(s):  
Reina Takeda ◽  
Shuhei Asada ◽  
Sung-Joon Park ◽  
Akihiko Yokoyama ◽  
Hans Jiro Becker ◽  
...  
Keyword(s):  
Insertional Mutagenesis ◽  
Ectopic Expression ◽  
Leukemia Cells ◽  
Sex Combs ◽  
Integration Sites ◽  
The Common ◽  
Additional Sex Combs ◽  
Induced Apoptosis ◽  
Retrovirus Integration ◽  
Modest Effect

Additional sex combs-like 1 (ASXL1), an epigenetic modulator, is frequently mutated in myeloid neoplasms. Recent analyses of mutant ASXL1 conditional knock-in (ASXL1-MT-KI) mice suggested that ASXL1-MT alone is insufficient for myeloid transformation. In our previous study, we utilized retrovirus-mediated insertional mutagenesis, which exhibited susceptibility of ASXL1-MT-KI hematopoietic cells to transform into myeloid leukemia cells. In this screening, we identified Hematopoietically expressed homeobox (HHEX) gene as one of the common retrovirus integration sites. In this study, we investigated the potential cooperation between ASXL1-MT and HHEX in myeloid leukemogenesis. Expression of HHEX enhanced proliferation of ASXL1-MT expressing HSPCs by inhibiting apoptosis and blocking differentiation, whereas it showed only modest effect in normal HSPCs. Moreover, ASXL1-MT and HHEX accelerated the development of RUNX1-ETO9a and FLT3-ITD leukemia. Conversely, HHEX depletion profoundly attenuated the colony-forming activity and leukemogenicity of ASXL1-MT-expressing leukemia cells. Mechanistically, we identified MYB and ETV5 as downstream targets for ASXL1-MT and HHEX by using transcriptome and ChIP-seq analyses. Moreover, we found that expression of ASXL1-MT enhanced the binding of HHEX to the promoter loci of MYB or ETV5 via reducing H2AK119ub. Depletion of MYB or ETV5 induced apoptosis or differentiation in ASXL1-MT-expressing leukemia cells, respectively. In addition, ectopic expression of MYB or ETV5 reversed the reduced colony-forming activity of HHEX-depleted ASXL1-MT-expressing leukemia cells. These findings indicated that the HHEX-MYB/ETV5 axis promotes myeloid transformation in ASXL1-mutated preleukemia cells.

scholarly journals Loss-of-function Additional sex combs like 1 mutations disrupt hematopoiesis but do not cause severe myelodysplasia or leukemia

Blood ◽  
2010 ◽  
Vol 115 (1) ◽  
pp. 38-46 ◽  
Author(s):  
Cynthia L. Fisher ◽  
Nicolas Pineault ◽  
Christy Brookes ◽  
Cheryl D. Helgason ◽  
Hideaki Ohta ◽  
...  
Keyword(s):  
Hox Genes ◽  
Homeodomain Protein ◽  
Loss Of Function ◽  
Genomic Amplification ◽  
Interaction Domain ◽  
Hematopoietic Stem ◽  
Amino Terminal ◽  
Sex Combs ◽  
Additional Sex Combs ◽  
Cell Fractions

Abstract The Additional sex combs like 1 (Asxl1) gene is 1 of 3 mammalian homologs of the Additional sex combs (Asx) gene of Drosophila. Asx is unusual because it is required to maintain both activation and silencing of Hox genes in flies and mice. Asxl proteins are characterized by an amino terminal homology domain, by interaction domains for nuclear receptors, and by a C-terminal plant homeodomain protein-protein interaction domain. A recent study of patients with myelodysplastic syndrome (MDS) and chronic myelomonocytic leukemia (CMML) revealed a high incidence of truncation mutations that would delete the PHD domain of ASXL1. Here, we show that Asxl1 is expressed in all hematopoietic cell fractions analyzed. Asxl1 knockout mice exhibit defects in frequency of differentiation of lymphoid and myeloid progenitors, but not in multipotent progenitors. We do not detect effects on hematopoietic stem cells, or in peripheral blood. Notably, we do not detect severe myelodysplastic phenotypes or leukemia in this loss-of-function model. We conclude that Asxl1 is needed for normal hematopoiesis. The mild phenotypes observed may be because other Asxl genes have redundant function with Asxl1, or alternatively, MDS or oncogenic phenotypes may result from gain-of-function Asxl mutations caused by genomic amplification, gene fusion, or truncation of Asxl1.

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