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1.
A novel ribosomal S6-kinase (RSK4; RPS6KA6) is commonly deleted in patients with complex X-linked mental retardation 总被引:8,自引:0,他引:8
Yntema HG van den Helm B Kissing J van Duijnhoven G Poppelaars F Chelly J Moraine C Fryns JP Hamel BC Heilbronner H Pander HJ Brunner HG Ropers HH Cremers FP van Bokhoven H 《Genomics》1999,62(3):332-343
Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM). The identification of deletions associated with classic CHM or DFN3 facilitated the positional cloning of the underlying genes, REP-1 and POU3F4, respectively, and enabled the positioning of the MRX gene in between these genes. Here, we report the cloning and characterization of a novel gene, ribosomal S6-kinase 4 (RSK4; HGMW-approved symbol RPS6KA6), which maps in the MRX critical region. RSK4 is completely deleted in eight patients with the contiguous gene syndrome including MRX, partially deleted in a patient with DFN3 and present in patients with an Xq21 deletion and normal intellectual abilities. RSK4 is most abundantly expressed in brain and kidney. The predicted protein of 746 amino acids shows a high level of homology to three previously isolated members of the human RSK family. RSK2 is involved in Coffin-Lowry syndrome and nonspecific MRX. The localization of RSK4 in the interval that is commonly deleted in mentally retarded males together with the high degree of amino acid identity with RSK2 suggests that RSK4 plays a role in normal neuronal development. Further mutation analyses in males with X-linked mental retardation must prove that RSK4 is indeed a novel MRX gene. 相似文献
2.
Summary Linkage studies and cytogenetically visible deletions associated with nonspecific X-linked mental retardation (XLMR) and a specific form of deafness (DFN3) have indicated that the genes responsible for these disorders are located at Xq21. Using DNA probes from this region, we have studied several overlapping deletions spanning different parts of Xq21. This has enabled us to assign the DFN3 gene and a gene for nonspecific XLMR to an interval that encompasses the locus DXS232 and that is flanked by DXS26 and DXS121. 相似文献
3.
Hela Ben Khelifa Najla Soyah Inesse Ben-Abdallah-Bouhjar Ryma Gritly Damien Sanlaville Hatem Elghezal Ali Saad Soumaya Mougou-Zerelli 《Gene》2013
X-linked ichthyosis is a genetic disorder affecting the skin and caused by a deficit in the steroid sulfatase enzyme (STS), often associated with a recurrent microdeletion at Xp22.31. Most of the STS deleted patients have X-linked ichthyosis as the only clinical feature and it is believed that patients with more complex disorders including mental retardation could be present as a result of contiguous gene deletion. In fact, VCX3A gene, a member of the VCX (variable charge, X chromosome) gene family, was previously proposed as the candidate gene for X-linked non-specific mental retardation in patients with X-linked ichthyosis. 相似文献
4.
Zeniou-Meyer M Gambino F Ammar MR Humeau Y Vitale N 《Cellular and molecular neurobiology》2010,30(8):1401-1406
Coffin-Lowry syndrome (CLS) is a syndromic form of X-linked mental retardation, characterized in male patients by psychomotor
and growth retardation and various skeletal anomalies. CLS is caused by mutations in the RPS6KA3 gene, which encodes RSK2, a growth factor-regulated protein kinase. Cognitive deficiencies in CLS patients are prominent,
but markedly variable in severity, even between siblings. However, the vast majority of patients are severely affected, with
mental retardation ranging from moderate to profound. We used a RSK2-KO mouse model that shows no obvious brain abnormalities
at the anatomical and histological levels to study the function of RSK2 in neurosecretion. Behavioral studies revealed normal
motor coordination, but a profound retardation in spatial learning and a deficit in long-term spatial memory, providing evidence
that RSK2 plays similar roles in mental functioning both in mice and human. We found that associative LTP at cortical inputs
to the lateral amygdala was blocked in Rsk2 KO mice. Using an RNA interference rescue strategy in PC12 cells, we were able to demonstrate that RSK2 regulates catecholamine
release through the phosphorylation of PLD. These results provide the first molecular evidence that RSK2 could regulate neurotransmitter
release by activating PLD production of lipids required for exocytosis. 相似文献
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7.
Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes 总被引:24,自引:0,他引:24
F P Cremers D J van de Pol P J Diergaarde B Wieringa R L Nussbaum M Schwartz H H Ropers 《Genomics》1989,4(1):41-46
Characterization of several male-viable deletions and duplications with 20 random DNA probes has enabled us to subdivide the Xq21 region into seven discernible intervals. Almost all of the deletions spanning part of Xq21 are associated with choroideremia and mental retardation, with deafness being another common feature. The gene locus for choroideremia was assigned to interval 3 spanning the loci DXS95, DXS165, and DXS233. Genes for X-linked deafness and mental retardation were tentatively assigned to interval 2. Deletions of intervals 4 through 7 were not associated with any clinical abnormality. We have constructed a preliminary long-range restriction map of intervals 2 and 3 using field-inversion gel electrophoresis. The DXS232, DXS121, and DXS233 loci are located on the same SfiI fragment, whereas the DXS165 and DXS95 loci could not be linked to this cluster using SfiI and SalI. 相似文献
8.
D. J. Wolff Karen M. Gustashaw Vickie Zurcher Lara Ko Wendy White Lester Weiss Daniel L. Van Dyke Stuart Schwartz Huntington F. Willard 《Human genetics》1997,100(2):256-262
High resolution cytogenetics, microsatellite marker analyses, and fluorescence in situ hybridization were used to define
Xq deletions encompassing the fragile X gene, FMR1, detected in individuals from two unrelated families. In Family 1, a 19-year-old
male had facial features consistent with fragile X syndrome; however, his profound mental and growth retardation, small testes,
and lover limb skeletal defects and contractures demonstrated a more severe phenotype, suggestive of a contiguous gene syndrome.
A cytogenetic deletion including Xq26.3–q27.3 was observed in the proband, his phenotypically normal mother, and his learning-disabled
non-dysmorphic sister. Methylation analyses at the FMR1 and androgen receptor loci indicated that the deleted X was inactive
in > 95% of his mother’s white blood cells and 80–85% of the sister’s leukocytes. The proximal breakpoint for the deletion
was approximately 10 Mb centromeric to FMR1, and the distal breakpoint mapped 1 Mb distal to FMR1. This deletion, encompassing
∼13 Mb of DNA, is the largest deletion including FMR1 reported to date. In the second family, a slightly smaller deletion
was detected. A female with moderate to severe mental retardation, seizures, and hypothyroidism, had a de novo cytogenetic
deletion extending from Xq26.3 to q27.3, which removed ∼12 Mb of DNA around the FMR1 gene. Cytogenetic and molecular data
revealed that ∼50% of her white blood cells contained an active deleted X. These findings indicate that males with deletions
including Xq26.3–q27.3 may exhibit a more severe phenotype than typical fragile X males, and females with similar deletions
may have an abnormal phenotype if the deleted X remains active in a significant proportion of the cells. Thus, important genes
for intellectual and neurological development, in addition to FMR1, may reside in Xq26.3–q27.3. One candidate gene in this
region, SOX3, is thought to be involved in neuronal development and its loss may partly explain the more severe phenotypes
of our patients.
Received: 19 December 1996 / Accepted: 13 March 1997 相似文献
9.
A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation
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Fukami M Kirsch S Schiller S Richter A Benes V Franco B Muroya K Rao E Merker S Niesler B Ballabio A Ansorge W Ogata T Rappold GA 《American journal of human genetics》2000,67(3):563-573
X-linked nonspecific mental retardation (MRX) has a frequency of 0.15% in the male population and is caused by defects in several different genes on the human X chromosome. Genotype-phenotype correlations in male patients with a partial nullisomy of the X chromosome have suggested that at least one locus involved in MRX is on Xp22.3. Previous deletion mapping has shown that this gene resides between markers DXS1060 and DXS1139, a region encompassing approximately 1.5 Mb of DNA. Analyzing the DNA of 15 males with Xp deletions, we were able to narrow this MRX critical interval to approximately 15 kb of DNA. Only one gene, VCX-A (variably charged, X chromosome mRNA on CRI-S232A), was shown to reside in this interval. Because of a variable number of tandem 30-bp repeats in the VCX-A gene, the size of the predicted protein is 186-226 amino acids. VCX-A belongs to a gene family containing at least four nearly identical paralogues on Xp22.3 (VCX-A, -B, -B1, and -C) and two on Yq11.2 (VCY-D, VCY-E), suggesting that the X and Y copies were created by duplication events. We have found that VCX-A is retained in all patients with normal intelligence and is deleted in all patients with mental retardation. There is no correlation between the presence or absence of VCX-B1, -B, and VCX-C and mental status in our patients. These results suggest that VCX-A is sufficient to maintain normal mental development. 相似文献
10.
S. Olinsky B. T. Loop A. DeKosky B. Ripepi W. Weng J. Cummins S. L. Wenger Y. Yan C. Lagenaur V. Narayanan 《Genomics》1996,33(3):532
M6 is a neuronal membrane glycoprotein that may have an important role in neural development. This molecule was initially defined by a monoclonal antibody that affected the survival of cultured cerebellar neurons and the outgrowth of neurites. The nature of the antigen was discovered by expression cDNA cloning using this monoclonal antibody. Two distinct murine M6 cDNAs (designated M6a and M6b) whose deduced amino acid sequences were remarkably similar to that of the myelin proteolipid protein were previously isolated. We have isolated partial human cDNA and genomic clones encoding M6a and M6b and have characterized them by restriction mapping, Southern hybridization with cDNA probes, and sequence analysis. We have localized these genes within the human genome by FISH (fluorescencein situhybridization). The human M6a gene is located at 4q34, and the M6b gene is located at Xp22.2. A number of human neurological disorders have been mapped to the Xp22 region, including Aicardi syndrome (MIM 304050), Rett syndrome (MIM 312750), X-linked Charcot–Marie–Tooth neuropathy (MIM 302801), and X-linked mental retardation syndromes (MRX1, MIM 309530). This raises the possibility that a defect in the M6b gene is responsible for one of these neurological disorders. 相似文献
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K. E. Davies M. G. Mattei J. F. Mattei H. Veenema S. McGlade K. Harper N. Tommerup K. B. Nielsen M. Mikkelsen P. Beighton D. Drayna R. White M. E. Pembrey 《Human genetics》1985,70(3):249-255
Summary One of the commonest forms of X-linked mental retardation is associated with a fragile site at Xq27 on the human X chromosome which can be visualised structurally after culturing cells in folate-deficient media. Unusually, the mutation can be transmitted through a phenotypically normal male. There is already some evidence that the gene loci for G6PD and factor IX are linked to this mental retardation locus. We have followed the inheritance of a DNA sequence 52A, in fragile site families that are also informative for factor IX. We demonstrate that these probes are localised at Xq27/Xq28-Xqter, close physically to the fragile site. We did not find close linkage between 52A, factor IX, and the fragile site in the families studied despite 52A and factor IX showing linkage in normal families. We discuss the importance of these data for the genetic mapping of this region of the human X chromosome and the implication for the use of these DNA probes for clinical diagnosis. 相似文献
13.
A gene for dominant nonspecific X-linked mental retardation is located in Xq28. 总被引:1,自引:0,他引:1
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V des Portes P Billuart A Carri L Bachner T Bienvenu M C Vinet C Beldjord G Ponsot A Kahn J Bou J Chelly 《American journal of human genetics》1997,60(4):903-909
A large family (MRX48) with a nonspecific X-linked mental retardation condition is described. An X-linked semidominant inheritance is suggested by the segregation in three generations of a moderate to severe mental retardation in seven males and by a milder intellectual impairment in two females, without any specific clinical, radiological, or biological feature. Two-point linkage analysis demonstrated significant linkage between the disorder and several markers in Xq28 (maximum LOD score [Zmax] = 2.71 at recombination fraction [theta] = 0); multipoint linkage analyses confirmed the significant linkage with a Zmax of 3.3 at theta = 0, at DXS1684. A recombination event observed with the flanking marker DXS8011 delineates a locus between this marker and the telomere. The approximate length of this locus is 8-9 cM, corresponding to 5.5-6 Mb. In an attempt to explain the variable intellectual impairment in females, we examined X-chromosome inactivation in all females of the family. Inactivation patterns in lymphocytes were random or moderately skewed, and no correlation between the phenotypic status and a specific inactivation pattern was observed. The interval of assignment noted in this family overlaps with five MRX loci previously reported in Xq28. 相似文献
14.
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3) 总被引:7,自引:3,他引:4
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I. Bach H. G. Brunner P. Beighton R. H. A. Ruvalcaba W. Reardon M. E. Pembrey S. D. van der Velde-Visser G. A. P. Bruns C. W. R. J. Cremers F. P. M. Cremers H.-H. Ropers 《American journal of human genetics》1992,51(1):38-44
Employing various probes from the proximal part of the Xq21 region, which is known to harbor the DFN3 gene, we have investigated 13 unrelated male probands with X-linked deafness, to detect possible deletions. For two of these patients, microdeletions could be detected by using probe pHU16 (DXS26). One of these deletions also encompasses locus DXS169, indicating that it extends farther toward the centromere. The presence of normal hybridization patterns in the DNA of 25 unrelated control males suggests that these deletions are the primary cause of progressive mixed deafness in these patients. If so, their molecular characterization may pave the way for the identification and isolation of the corresponding gene. 相似文献
15.
FACL4, a New Gene Encoding Long-Chain Acyl-CoA Synthetase 4, Is Deleted in a Family with Alport Syndrome, Elliptocytosis, and Mental Retardation 总被引:1,自引:0,他引:1
Monica Piccini Francesca Vitelli Mirella Bruttini Barbara R. Pober Jon J. Jonsson Marcello Villanova Massimo Zollo Giuseppe Borsani Andrea Ballabio Alessandra Renieri 《Genomics》1998,47(3):350
16.
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencing
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J. A. J. M. van den Hurk T. J. R. van de Pol C. M. Molloy F. Brunsmann K. Rüther E. Zrenner A. J. L. G. Pinckers I. H. Pawlowitzki E. M. Bleeker-Wagemakers B. Wieringa H. -H. Ropers F. P. M. Cremers 《American journal of human genetics》1992,50(6):1195-1202
By making use of positional cloning strategies we recently isolated a candidate gene for choroideremia (CHM), which is transcribed in retina, choroid, and/or retinal pigment epithelium. The gene contains an open reading frame that is structurally altered in 10 CHM patients with sizable deletions and in a female patient with a balanced translocation involving the Xq21 band. Employing PCR-SSCP analysis and direct DNA sequencing we have now detected and characterized different point mutations in five patients with CHM. Each of these mutations introduces a termination codon into the open reading frame of the CHM candidate gene, thereby predicting a distinct truncated protein product. Together these findings provide convincing evidence for the candidate gene being identical with the choroideremia gene. 相似文献
17.
Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation
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Shoichet SA Hoffmann K Menzel C Trautmann U Moser B Hoeltzenbein M Echenne B Partington M Van Bokhoven H Moraine C Fryns JP Chelly J Rott HD Ropers HH Kalscheuer VM 《American journal of human genetics》2003,73(6):1341-1354
18.
The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK 总被引:12,自引:2,他引:10
Han G. Brunner Cor A. van Bennekom Eric M. M. Lambermon T. Lian Oei Cor W. R. J. Cremers Bé Wieringa Hans-Hilger Ropers 《Human genetics》1988,80(4):337-340
Summary A linkage analysis has been performed in a large Dutch kindred with progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) using a panel of X-chromosomal RFLPs. Tight linkage (zmax=3.07 at =0.00) was demonstrated with the locus for phosphoglycerate kinase (PGK), which is located at Xq13. Tight linkage was excluded for DXS9 (probe RC8) and DXS41 (probe 99.6) on Xp and for blood clotting factor 9 (FIX) on distal Xq. Deafness is one of the predominant clinical features in males with deletions of the Xq21 band. Our results suggest that this association may be due to involvement of the DFN3 gene. 相似文献
19.
Summary Twelve fibroblast clones from two males with X-linked mental retardation expressed the fragile site Xq27 in 3%–38% of metaphases analyzed. The number of in vitro doublings during the cloning procedure had no evident influence on the induction of fragile X expression. The variability of fragile X expression seems to depend on cell properties acquired during culture rather than on properties originally inherent in the cells. 相似文献
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