116 research outputs found
Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2
Kallmann syndrome combines anosmia, related to defective olfactory bulb morphogenesis, and hypogonadism due to gonadotropin-releasing hormone deficiency. Loss-of-function mutations in KAL1 and FGFR1 underlie the X chromosome-linked form and an autosomal dominant form of the disease, respectively. Mutations in these genes, however, only account for approximately 20% of all Kallmann syndrome cases. In a cohort of 192 patients we took a candidate gene strategy and identified ten and four different point mutations in the genes encoding the G protein-coupled prokineticin receptor-2 (PROKR2) and one of its ligands, prokineticin-2 (PROK2), respectively. The mutations in PROK2 were detected in the heterozygous state, whereas PROKR2 mutations were found in the heterozygous, homozygous, or compound heterozygous state. In addition, one of the patients heterozygous for a PROKR2 mutation was also carrying a missense mutation in KAL1, thus indicating a possible digenic inheritance of the disease in this individual. These findings reveal that insufficient prokineticin-signaling through PROKR2 leads to abnormal development of the olfactory system and reproductive axis in man. They also shed new light on the complex genetic transmission of Kallmann syndrome
MSY Breakpoint Mapper, a database of sequence-tagged sites useful in defining naturally occurring deletions in the human Y chromosome
Y chromosome deletions arise frequently in human populations, where they cause sex reversal and Turner syndrome and predispose individuals to infertility and germ cell cancer. Knowledge of the nucleotide sequence of the male-specific region of the Y chromosome (MSY) makes it possible to precisely demarcate such deletions and the repertoires of genes lost, offering insights into mechanisms of deletion and the molecular etiologies of associated phenotypes. Such deletion mapping is usually conducted using polymerase chain reaction (PCR) assays for the presence or absence of a series of Y-chromosomal DNA markers, or sequence-tagged sites (STSs). In the course of mapping intact and aberrant Y chromosomes during the past two decades, we and our colleagues have developed robust PCR assays for 1287 Y-specific STSs. These PCR assays amplify 1698 loci at an average spacing of <14 kb across the MSY euchromatin. To facilitate mapping of deletions, we have compiled a database of these STSs, MSY Breakpoint Mapper (http://breakpointmapper.wi.mit.edu/). When queried, this online database provides regionally targeted catalogs of STSs and nearby genes. MSY Breakpoint Mapper is useful for efficiently and systematically defining the breakpoint(s) of virtually any naturally occurring Y chromosome deletion.National Institutes of Health (U.S.)Howard Hughes Medical Institut
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis
<p>Abstract</p> <p>Background</p> <p>Usher syndrome (USH) combines sensorineural deafness with blindness. It is inherited in an autosomal recessive mode. Early diagnosis is critical for adapted educational and patient management choices, and for genetic counseling. To date, nine causative genes have been identified for the three clinical subtypes (USH1, USH2 and USH3). Current diagnostic strategies make use of a genotyping microarray that is based on the previously reported mutations. The purpose of this study was to design a more accurate molecular diagnosis tool.</p> <p>Methods</p> <p>We sequenced the 366 coding exons and flanking regions of the nine known USH genes, in 54 USH patients (27 USH1, 21 USH2 and 6 USH3).</p> <p>Results</p> <p>Biallelic mutations were detected in 39 patients (72%) and monoallelic mutations in an additional 10 patients (18.5%). In addition to biallelic mutations in one of the USH genes, presumably pathogenic mutations in another USH gene were detected in seven patients (13%), and another patient carried monoallelic mutations in three different USH genes. Notably, none of the USH3 patients carried detectable mutations in the only known USH3 gene, whereas they all carried mutations in USH2 genes. Most importantly, the currently used microarray would have detected only 30 of the 81 different mutations that we found, of which 39 (48%) were novel.</p> <p>Conclusions</p> <p>Based on these results, complete exon sequencing of the currently known USH genes stands as a definite improvement for molecular diagnosis of this disease, which is of utmost importance in the perspective of gene therapy.</p
Accessory tubules and axonemal microtubules of Apis mellifera sperm flagellum differ in their tubulin isoform content.
In the insect sperm flagellum, an extra set of nine additional microtubules, named
accessory tubules, is present surrounding the axoneme. Using a sarcosyl/urea extraction,
we were able to fractionate the microtubular cytoskeleton of the sperm flagellum
of the insect Apis mellifera resulting in the dissociation of the axonemal microtubule
protein components and the accessory tubules. This has allowed us to compare the
tubulin isoform content of axonemal microtubules and accessory tubules by immunoelectron
microscopy and immunoblotting using a panel of monoclonal antibodies
directed against different tubulin post-translational modifications (PTMs). All the
PTMs occurring in axonemal tubulin are also present in accessory tubules, which
indicates the close relativeness of accessory tubules to axonemal rather than to
cytoplasmic microtubules. However, our results demonstrate the presence of significant
differences in the tubulin isoform content of axonemal microtubules and accessory
tubules. First, the tubulin tyrosination extent of accessory tubules is far lower than
that of axonemal microtubules, thus confirming at the molecular level their morphogenetic
origin as outgrowths from the B-subtubule of each microtubular doublet.
Second, although polyglycylation seems to occurr at the same extent in both microtubular
systems, a-tubulin exhibits a larger amount of monoglycylated sites in axonemal
microtubules than in accessory tubules. Third, a greater amount of b-tubulin
molecules is glutamylated in axonemal microtubules than in accessory tubules. Moreover,
highly acidic isoforms, likely molecules with longer polyglutamate side chains,
are present only in axonemal microtubules. Taken together, our data are indicative of
a higher level of tubulin heterogeneity in axonemal microtubules than in accessory
tubules. They also show a segregation of post-translationally modified isoforms
between accessory tubules and axonemal microtubules and suggest the implication of
PTMs in the functional specialization of the two microtubular systems
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