Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UNIPROT:P06889 (Mol)
 630,302 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The reproductive physiology of Corynorhinus mexicanus includes a testes growth-involution cycle. Testis recrudescence begins in May-June, peaks in August and then undergoes a profound involution being totally regressed in November. Adult, male individuals were captured monthly during one year and ROS scavenging enzyme activities were measured in testes and expressed per total wet-weight and per mg protein. SOD total activity is very low from October to February; increases sharply one full month before testes recrudescence starts, and in August, when testis activity was at its peak, SOD is 3-4 times lower than in July. Catalase total activity is bimodal. The main peak of activity occurs during testicular recrudescence with an additional smaller peak, two months before the onset of recrudescence. Glutathione peroxidase total activity parallels almost exactly the testis growth cycle, increases in July, reaches a peak in August and decreases through September to almost disappear in October. SOD specific activity shows a pre-testicular increase of activity, maintains its activity from March to July and then descends drastically to almost nil in August, maintaining these low values until February. Catalase specific activity is particularly important during the period of testicular regression. GPX specific activity is low from March to July, months of testicular recrudescence; whereas its activity increases in August and peaks in November, when testes regression occurs. Our data show that ROS-scavenging enzymes may play a very important role during testes involution-recrudescence in C. mexicanus, and we believe their participation could be equally important in all seasonally breeding mammals.
Comp Biochem Physiol A Mol Integr Physiol 2007 Sep
PMID:Superoxide dismutase, catalase, and glutathione peroxidase in the testis of the Mexican big-eared bat (Corynorhinus mexicanus) during its annual reproductive cycle. 1748 34

Kinesins are a superfamily of microtubule-based motors that power intracellular traffic and play important roles in many fundamental cellular and developmental processes. Kinesins move on microtubules from their minus to plus end (conventional kinesin) or from plus to minus end (C-terminal kinesins), carrying cargoes to different destinations. A variety of cargoes such as vesicles, proteins, lipid drops, pigments, and the nucleus are moved by kinesins along cytoplasmic microtubules. Multiple mitotic kinesins and microtubule-associated proteins (MAPs) also have direct functions in spindle formation, chromosome segregation, and cytokinesis. Spermatogenesis provides an excellent model system to study the role of kinesin motor proteins during the dramatic cytoskeletal rearrangements that take place during male germ cell development. This chapter describes how to identify the multiple functions of kinesin motors during spermatogenesis by using ultrastructural analysis. Testis perfusion is described in detail, including how to anesthetize animals and how to select seminiferous tubules under transilluminated microscopy. Practical immunocytochemical staining is also described in detail in this chapter, especially methods to enhance staining and avoid contamination.
Methods Mol Biol 2007
PMID:Ultrastructural analysis of kinesin-related motor proteins during spermatogenesis. 1795 15

Easy oocyte detection in living specimens benefits various developmental biology and environmental toxicology studies. One of the earliest markers of sex differentiation in medaka (Oryzias latipes) is oocyte development. Within the field of toxicology, a simple detection method for induced oocyte in the testis (testis-ova) as a result of endocrine disruption is necessary. In this study we produced transgenic medaka whose oocytes were labeled with fluorescent proteins using the regulatory region of the 42Sp50 gene, an isoform of polypeptide elongation 1-alpha. Short (201 nt) 5'- and 3'-flanking regions were sufficient for reporter gene expression. GFP expression was first observed in female germ cells approximately 5 days post-hatching. In the mature ovaries, germ cells showed such intense fluorescence that the fluorescence was observed from outside the body wall. In contrast, very faint fluorescence was observed in the mature testes. Testis-ova, oocytes artificially induced in the testes, were also labeled with GFP. These findings indicate through the use of transgenic medaka, that detection of female germ cells was straightforward and this transgenic medaka model proves useful for tracking female germ cells in developmental and toxicological studies.
Mol Reprod Dev 2009 Feb
PMID:Transgenic medaka enables easy oocytes detection in live fish. 1854 84

The majority of the audience at the European Testis Workshop were actively researching mammalian spermatogenesis or sperm function. In this paper therefore I follow the brief I had for my contribution to the meeting in the session "non-mammalian models of spermatogenesis", which was to explain practical approaches to research in Drosophila spermatogenesis, illuminating how what we learn in model organisms can be relevant to male fertility research in mammals. I discuss techniques and resources available to fly spermatogenesis researchers, and indicate how I have applied them in my lab to understand regulation of gene expression in spermatogenesis.
Mol Cell Endocrinol 2009 Jul 10
PMID:Studying how flies make sperm--investigating gene function in Drosophila testes. 1910 6

Males of Limnogonus aduncus were found to have the sex chromosome system X0 and chromosome number 2n = 23 (22A + X0). Testis cells were stained with lacto-acetic orcein and silver nitrate so that changes in the morphology and degree of staining of the heteropicnotic chromatin and the nucleolar material could be observed during meiosis and spermiogenesis. These structures share the same nuclear position and could be seen until almost the end of spermiogenesis. A chromosome region stained with silver nitrate was indicative of a nucleolar organizing region (NOR), which is rarely detected in Heteroptera with this technique. The NOR is located at one end of a single member of an autosome pair. The finding of this stained region enabled us to observe that the telomeric association of sister chromatids that characterizes the Heteroptera does not include the chromosome ends, where NORs are located; we also observed in anaphase that the chromosome end through which it is pulled to the pole is the one containing the NOR. Another observation was that the single nucleolar body present in the cells at anaphase never goes to the cell pole that does not receive the NOR. We conclude that L. aduncus is a good model for cytogenetic studies involving nucleolar activity and also may be useful for studying the mechanisms of activation and inactivation of kinetic activity at the chromosome ends. Although the chromosomes of Heteroptera are known to be holocentric, whether kinetic activity is restricted to one or involves both chromosome ends is still not well understood.
Genet Mol Res 2008 Dec 16
PMID:Heteropicnotic chromatin and nucleolar activity in meiosis and spermiogenesis of Limnogonus aduncus (Heteroptera, Gerridae): a stained nucleolar organizing region that can serve as a model for studying chromosome behavior. 1922 57

Testis-derived germline stem (GS) cells can undergo re-programming to acquire multipotency when cultured under appropriate culture conditions. These multipotent GS (mGS) cells have been known to differ from GS cells in their DNA methylation pattern. In this study, we examined the DNA methylation status of the H19 imprinting control region (ICR) in multipotent adult germline stem (maGS) cells to elucidate how epigenetic imprints are altered by culture conditions. DNA methylation was analyzed by bisulfite sequencing PCR of established maGS cells cultured in the presence of glial cell line-derived neurotrophic factor (GDNF) alone or both GDNF and leukemia inhibitory factor (LIF). The results showed that the H19 ICR in maGS cells of both groups was hypermethylated and had an androgenetic pattern similar to that of GS cells. In line with these data, the relative abundance of the Igf2 mRNA transcript was two-fold higher and that of H19 was three fold lower than in control embryonic stem cells. The androgenetic DNA methylation pattern of the H19 ICR was maintained even after 54 passages. Furthermore, differentiating maGS cells from retinoic acid-treated embryoid bodies maintained the androgenetic imprinting pattern of the H19 ICR. Taken together these data suggest that our maGS cells are epigenetically stable for the H19 gene during in vitro modifications. Further studies on the epigenetic regulation and chromatin structure of maGS cells are therefore necessary before their full potential can be utilized in regenerative medicine.
Mol Cells 2009 Jun 30
PMID:H19 gene is epigenetically stable in mouse multipotent germline stem cells. 1953 39

Maintenance of sex-specific germ cells requires balanced activation and repression of genetic hierarchies to ensure gender-appropriate development in mammals. Figla (factor in the germ line, alpha) encodes a germ cell-specific basic helix-loop-helix transcription factor first identified as an activator of oocyte genes. In comparing the ovarian proteome of normal and Figla null newborn mice, 18 testis-specific or -enhanced proteins were identified that were more abundant in Figla null ovaries than in normal ovaries. Transgenic mice, ectopically expressing Figla in male germ cells, downregulated a subset of these genes and demonstrated age-related sterility associated with impaired meiosis and germ cell apoptosis. Testis-associated genes, including Tdrd1, Tdrd6, and Tdrd7, were suppressed in the transgenic males with a corresponding disruption of the sperm chromatoid body and mislocalization of MVH and MILI proteins, previously implicated in posttranscriptional processing of RNA. These data demonstrate that physiological expression of Figla plays a critical dual role in activation of oocyte-associated genes and repression of sperm-associated genes during normal postnatal oogenesis.
Mol Cell Biol 2010 Jul
PMID:FIGLA, a basic helix-loop-helix transcription factor, balances sexually dimorphic gene expression in postnatal oocytes. 2047 25

We looked for a possible association between Klinefelter syndrome (KFS) and microdeletions in the Y chromosome in Turkish KFS patients. We examined the frequency of KFS in male patients with proven non-obstructive azoospermia and the types of Y chromosome microdeletions in these KFS patients. Fifty azoospermic patients and 50 fertile men were included in this study. KFS was found in 14 azoospermic patients. Y chromosome microdeletions were found in eight KFS patients. Azoospermia factor locus c (AZFc) was the most commonly deleted interval in KFS patients. All KFS patients had elevated plasma follicle-stimulating hormone and luteinizing hormone concentrations, but they had normal plasma testosterone concentrations. Testis biopsy of five samples with Y microdeletions revealed Sertoli cell-only syndrome. No Y microdeletions were found in the fertile group. We concluded that there could be an association between the AZFc region and KFS. Screening for this should be part of diagnostic work-up, particularly in those considering assisted reproduction.
Genet Mol Res 2010 Jun 29
PMID:The azoospermia factor locus-c region was found to be related to Klinefelter syndrome in Turkish patients. 2060 8

The X chromosome plays an important role in both adaptive evolution and speciation. We used a molecular evolutionary screen of X-linked genes potentially involved in reproductive isolation in mice to identify putative targets of recurrent positive selection. We then sequenced five very rapidly evolving genes within and between several closely related species of mice in the genus Mus. All five genes were involved in male reproduction and four of the genes showed evidence of recurrent positive selection. The most remarkable evolutionary patterns were found at Testis-specific gene a8 (Tsga8), a spermatogenesis-specific gene expressed during postmeiotic chromatin condensation and nuclear transformation. Tsga8 was characterized by extremely high levels of insertion-deletion variation of an alanine-rich repetitive motif in natural populations of Mus domesticus and M. musculus, differing in length from the reference mouse genome by up to 89 amino acids (27% of the total protein length). This population-level variation was coupled with striking divergence in protein sequence and length between closely related mouse species. Although no clear orthologs had previously been described for Tsga8 in other mammalian species, we have identified a highly divergent hypothetical gene on the rat X chromosome that shares clear orthology with the 5' and 3' ends of Tsga8. Further inspection of this ortholog verified that it is expressed in rat testis and shares remarkable similarity with mouse Tsga8 across several general features of the protein sequence despite no conservation of nucleotide sequence across over 60% of the rat-coding domain. Overall, Tsga8 appears to be one of the most rapidly evolving genes to have been described in rodents. We discuss the potential evolutionary causes and functional implications of this extraordinary divergence and the possible contribution of Tsga8 and the other four genes we examined to reproductive isolation in mice.
Mol Biol Evol 2011 May
PMID:Extraordinary sequence divergence at Tsga8, an X-linked gene involved in mouse spermiogenesis. 2118 89

The testis is a heterogeneous organ that comprises a number of cell types, including germ cells at -different stages in their maturation, differentiated neighbor nursing cells, and endocrine somatic cells. Despite such cellular heterogeneity the testis is highly organized, with germ cell development and differentiation being compartmentalized into the interconnected tubular network of the seminiferous epithelium. Intratesticular scaffolds rely heavily on the basement membrane of the seminiferous tubules while germ cell development inside the seminiferous epithelium is critically dependent on the Blood Testis Barrier (BTB). The BTB is a macromolecular tight junction complex generated by somatic Sertoli cells within the seminiferous epithelium. The BTB divides the seminiferous epithelium into two compartments: the basal compartment, which delineates a niche for the proliferation and renewal of spermatogonia; and the adluminal compartment, where differentiating germ cells undergo meiosis and spermiogenesis. The BTB is unique in mammalian tissues because it is cyclically reconstructed during the spermatogenic cycle as preleptotene spermatocytes migrate from the basal compartment to the adluminal compartment and enter meiosis. In mouse, the loss of the BTB in the absence of the claudin 11 protein causes azoospermia and leads to infertility. Specifically, cldn11 deficiency results in sloughing of the cells of the seminiferous epithelium into the lumen. Understanding this pathophysiology has involved histological examination of the tissue defects as well as immunohistological characterization. Here, we present a comparative study of several modifications to the classical Hematoxylin-Eosin stain that may improve the diagnostic usefulness of this technique, as well as the use of several selective markers to identify testicular cell types.
Methods Mol Biol 2011
PMID:Phenotyping the claudin 11 deficiency in testis: from histology to immunohistochemistry. 2187 55


<< Previous 1 2 3 4 5 6 7 Next >>