205 research outputs found

    Entangled Stories: The Red Jews in Premodern Yiddish and German Apocalyptic Lore

    Get PDF
    “Far, far away from our areas, somewhere beyond the Mountains of Darkness, on the other side of the Sambatyon River…there lives a nation known as the Red Jews.” The Red Jews are best known from classic Yiddish writing, most notably from Mendele's Kitser masoes Binyomin hashlishi (The Brief Travels of Benjamin the Third). This novel, first published in 1878, represents the initial appearance of the Red Jews in modern Yiddish literature. This comical travelogue describes the adventures of Benjamin, who sets off in search of the legendary Red Jews. But who are these Red Jews or, in Yiddish, di royte yidelekh? The term denotes the Ten Lost Tribes of Israel, the ten tribes that in biblical times had composed the Northern Kingdom of Israel until they were exiled by the Assyrians in the eighth century BCE. Over time, the myth of their return emerged, and they were said to live in an uncharted location beyond the mysterious Sambatyon River, where they would remain until the Messiah's arrival at the end of time, when they would rejoin the rest of the Jewish people. This article is part of a broader study of the Red Jews in Jewish popular culture from the Middle Ages through modernity. It is partially based on a chapter from my book, Umstrittene Erlöser: Politik, Ideologie und jüdisch-christlicher Messianismus in Deutschland, 1500–1600 (Göttingen: Vandenhoeck & Ruprecht, 2011). Several postdoctoral fellowships have generously supported my research on the Red Jews: a Dr. Meyer-Struckmann-Fellowship of the German Academic Foundation, a Harry Starr Fellowship in Judaica/Alan M. Stroock Fellowship for Advanced Research in Judaica at Harvard University, a research fellowship from the Heinrich Hertz-Foundation, and a YIVO Dina Abramowicz Emerging Scholar Fellowship. I thank the organizers of and participants in the colloquia and conferences where I have presented this material in various forms as well as the editors and anonymous reviewers of AJS Review for their valuable comments and suggestions. I am especially grateful to Jeremy Dauber and Elisheva Carlebach of the Institute for Israel and Jewish Studies at Columbia University, where I was a Visiting Scholar in the fall of 2009, for their generous encouragement to write this article. Sue Oren considerably improved my English. The style employed for Romanization of Yiddish follows YIVO's transliteration standards. Unless otherwise noted, translations from the Yiddish, Hebrew, German, and Latin are my own. Quotations from the Bible follow the JPS translation, and those from the Babylonian Talmud are according to the Hebrew-English edition of the Soncino Talmud by Isidore Epstein

    The C313Y Piedmontese mutation decreases myostatin covalent dimerisation and stability

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Myostatin is a key negative regulator of muscle growth and development, whose activity has important implications for the treatment of muscle wastage disorders. Piedmontese cattle display a double-muscled phenotype associated with the expression of C313Y mutant myostatin. <it>In vivo</it>, C313Y myostatin is proteolytically processed, exported and circulated extracellularly but fails to correctly regulate muscle growth. The C313Y mutation removes the C313-containing disulphide bond, an integral part of the characteristic TGF-β cystine-knot structural motif.</p> <p>Results</p> <p>Here we present <it>in vitro </it>analysis of the structure and stability of the C313Y myostatin protein that reveals significantly decreased covalent dimerisation for C313Y myostatin accompanied by a loss of structural stability compared to wild type. The C313Y myostatin growth factor, processed from full length precursor protein, fails to inhibit C2C12 myoblast proliferation in contrast to wild type myostatin. Although structural modeling shows the substitution of tyrosine causes structural perturbation, biochemical analysis of additional disulphide mutants, C313A and C374A, indicates that an intact cystine-knot motif is a major determinant in myostatin growth factor stability and covalent dimerisation.</p> <p>Conclusions</p> <p>This research shows that the cystine-knot structure is important for myostatin dimerisation and stability, and that disruption of this structural motif perturbs myostatin signaling.</p

    Transient up- and down-regulation of expression of myosin light chain 2 and myostatin mRNA mark the changes from stratified hyperplasia to muscle fiber hypertrophy in larvae of gilthead sea bream (Sparus aurata L.)

    Get PDF
    Hyperplasia and hypertrophy are the two mechanisms by which muscle develops and grows. We study these two mechanisms, during the early development of white muscle in Sparus aurata, by means of histology and the expression of structural and regulatory genes. A clear stage of stratified hyperplasia was identified early in the development of gilthead sea bream but ceased by 35 dph when hypertrophy took over. Mosaic recruitment of new white fibers began as soon as 60 dph. The genes mlc2a and mlc2b were expressed at various levels during the main phases of hyperplasia and hypertrophy. The genes myog and mlc2a were significantly up-regulated during the intensive stratified formation of new fibers and their expression was significantly correlated. Expression of mstn1 and igf1 increased at 35 dph, appeared to regulate the hyperplasia-to-hypertrophy transition, and may have stimulated the expression of mlc2a, mlc2b and col1a1 at the onset of mosaic hyperplasia. The up-regulation of mstn1 at transitional phases in muscle development indicates a dual regulatory role of myostatin in fish larval muscle growth

    Protandrous Hermaphroditism In Australian Silver Perch, Bidyanus Bidyanus (Mitchell, 1836)

    Get PDF
    Gonadal development in two progenies of the Australian silver perch, Bidyanus bidyanus, was studied from the larval stage to 18.5 months. For approximately one month after hatching, it was impossible to visually or histologically determine the sex of the fish. Two to three months after hatching, anatomical and cytological sex differentiation occurred. At 4-5 months, the testis in most of the fish longer than 7-8 cm exhibited all stages of spermatogenesis including spermatozoa. Very few females were found among the 4 and 6.5 month fish. Up to 18.5 months, 7.1-23.5% were female (except in one batch). There were only 25 females, all at early stages of oogenesis, amongst 204 fish with differentiated sex gonads. In 10 of 17 histologically studied females, there were degenerating male cells (possibly spermatocytes) among a majority of developing oocytes. The predominance of phenotypic males, and the occurrence of females with ovaries and degen- erating male cells, indicate that during the first years of life, this species is a protandrous her- maphrodite. The testis develops during ontogenesis in a direct manner, whereas the female gonad develops indirectly, passing through an intermediate masculine stage

    Cellular distribution of insulin-like growth factor II (IGF-II) mRNA and hormonal regulation of IGF-I and IGF-II mRNA expression in rainbow trout testis (Oncorhynchus mykiss)

    No full text
    International audienceIn this study, Northern blot analysis of RNA from trout testis revealed a single transcript of insulin-like growth factor II (IGF-II) around 4.7 kb. The cellular distribution of IGF-II mRNA was studied and quantified in different testicular cells enriched populations by RT-PCR. IGF-II mRNA appears to be expressed in all cellular types tested: spermatogonia A and B, primary spermatocytes, spermatids and secondary spermatocytes and Sertoli cells. A significantly higher expression of IGF-II was found in premeiotic germ cells. The levels of IGF-LI mRNA appear to be higher than those of IGF-I in immature trout testis, as judged from the semi-quantitative RT-PCR results. These data suggest that in addition to IGF-I, IGF-II may play a role in testicular physiology in fish.The hormonal regulation of IGF-I and IGF-II gene expression was investigated both in vitro and in vivo using RT-PCR approach. Gonadotropin (GtH) added to testicular explants increased IGF-II mRNA levels but had no effect on IGF-I. No statistically significant effect was observed with androgens. In vivo, GH and pituitary extracts resulted in an 8 fold and 2-3 fold increase in both IGF-I and IGF-II mRNA levels, respectively.Taken together, our study suggests that IGF-I and IGF-LT may act as local mediators of GH and GtHs in fish testis. Moreover, our results imply that in fish testicular cells, IGFs are potential paracrine/autocrine regulators inside the spermatogenic compartment and can act directly on germ cells to stimulate their proliferation

    Piscine (Sparus aurata) α subunit of the G-protein transducin is homologous to mammalian cone and rod transducin

    Get PDF
    AbstractA novel cDNA encoding α subunit of the GTP-binding protein, transducin, has been cloned from a marine fish, Sparus aurata. The cDNA contains an open reading frame of 1050 nt (encoding 350 amino acid residues). A high degree of identity was found with known mammalian transducin proteins of cones (Gt2α) or rods (Gt1α): human Gt2α (80.2%), bovine Gt2α (79.3%), mouse Gt1α (78.2%), mouse Gt2α (78%) and bovine Gt1α (77.9%). Northern blot analysis of different tissues revealed a transcript of about 2.5 kb, which is expressed only in the fish eye and not in other tissues from adult fish, supporting its identification as transducin. Ontogeny of transducin mRNA expression during early development of Sparus aurata, determined by Northern blot analysis, showed very low levels in larvae 3 days after hatching but not earlier. Levels increased 3- and 6-fold on days 4 and 6 (respectively) compared with those on day 3 and remained essentially unchanged thereafter, until day 21 after hatching (the last day studied). Our results suggest that in fish only one α subunit of transducin is found, which shows similar identity with cone and rod α subunits of mammals

    Protandrous Hermaphroditism In Australian Silver Perch, Bidyanus Bidyanus (Mitchell, 1836)

    No full text
    Gonadal development in two progenies of the Australian silver perch, Bidyanus bidyanus, was studied from the larval stage to 18.5 months. For approximately one month after hatching, it was impossible to visually or histologically determine the sex of the fish. Two to three months after hatching, anatomical and cytological sex differentiation occurred. At 4-5 months, the testis in most of the fish longer than 7-8 cm exhibited all stages of spermatogenesis including spermatozoa. Very few females were found among the 4 and 6.5 month fish. Up to 18.5 months, 7.1-23.5% were female (except in one batch). There were only 25 females, all at early stages of oogenesis, amongst 204 fish with differentiated sex gonads. In 10 of 17 histologically studied females, there were degenerating male cells (possibly spermatocytes) among a majority of developing oocytes. The predominance of phenotypic males, and the occurrence of females with ovaries and degen- erating male cells, indicate that during the first years of life, this species is a protandrous her- maphrodite. The testis develops during ontogenesis in a direct manner, whereas the female gonad develops indirectly, passing through an intermediate masculine stage.</jats:p
    corecore