Genetic characterization of Acipenser sturio L., 1758 in relation to other sturgeon species using satellite DNA

We obtained and characterized a satellite (st) DNA family named HindIII from the genomes of the Adriatic sturgeon Acipenser naccarii Bonaparte, 1836, Siberian sturgeon Acipenser baerii Brandt, 1869, and beluga sturgeon Huso huso (L., 1758). We did not find this stDNA in the genome of the Atlantic sturgeon Acipenser sturio L., 1758. The comparison of sturgeon species using the HindIII stDNA revealed the following: (1) A. naccarii and A. baerii are closely related; (2) H. huso appears to belong to the genus Acipenser and, probably, Huso is not a separate genus within the Acipenserinae; (3) A. sturio differs from the other three studied species by the absence of the HindIII stDNA and, most likely, it represents a separate evolutionary lineage within the Acipenseridae. The data on the HindIII stDNA can be successfully used for species identification of sturgeon specimens captured in different European regions.En este trabajo presentamos la caracterización del genoma de Acipenser sturio L., 1758 en relación con el genoma de Acipenser naccarii Bonaparte, 1836, Acipenser baerii Brandt, 1869 y Huso huso (L., 1758) utilizando una familia de ADN satélite (la familia HindIII). Nuestro análisis revela que: (1) A. naccarii y A. baerii son especies muy emparentadas; (2) H. huso aparece muy relacionada con las especies del género Acipenser y, probablemente, podría ser considerada como una especie perteneciente a dicho género, y (3) A. sturio difiere del resto de las especies analizadas, lo que sugiere que esta especie ha debido seguir una evolución independiente respecto a las otras especies. Estos datos pueden ser muy útiles, no sólo para establecer las relaciones filogenéticas entre A. sturio y las otras especies de Acipenseridae, sino también para la identificación de ejemplares de esturiones capturados en diferentes regiones europeas.Instituto Español de Oceanografí

Morphometric and genetic analysis as proof of the existence of two sturgeon species in the Guadalquivir river

Morphometric and genetic methods were used to identify two sturgeon species, Acipenser naccarii Bo- naparte, 1836, and A. sturio Linnaeus, 1758, captured in some of the principal rivers of the Iberian Peninsula, including the Guadalquivir. After measuring 25 Iberian specimens from a ®shery and several Spanish and Por- tuguese museums and applying stepwise discriminant analysis (SDA), four specimens preserved in di erent museums [two specimens from the Guadalquivir river (EBD-8173 and EBD-8174), one specimen from the Tagus river (MUC1) and one specimen from the Mondego river (MUC46B)], as well as ®ve specimens captured in the Guadalquivir river in the 1940s but not preserved (CM1, CM2, CM3, CM4 and CM5), were identi®ed as A. naccarii. After cloning and character- isation of a satellite-DNA family, HindIII, from A. naccarii genome, its absence from the genome of A. sturio was determined. Using this satellite-DNA as a genetic marker and by means of dot-blotting, we dem- onstrate that the DNA of the two specimens captured during the mid-1970s in the Guadalquivir river cross- hybridised with HindIII satellite-DNA sequences of A. naccarii. We conclude that A. naccarii is autochtho- nous to the Iberian Peninsula and is not, as was previ- ously believed, endemic to the Adriatic Sea

A novel Carcinoembryonic Antigen (CEA)-Targeted Trimeric Immunotoxin shows signifcantly enhanced Antitumor Activity in Human Colorectal Cancer Xenografts

Immunotoxins are chimeric molecules, which combine antibody specifcity to recognize and bind with high-afnity tumor-associated antigens (TAA) with the potency of the enzymatic activity of a toxin, in order to induce the death of target cells. Current immunotoxins present some limitations for cancer therapy, driving the need to develop new prototypes with optimized properties. Herein we describe the production, purifcation and characterization of two new immunotoxins based on the gene fusion of the anti-carcinoembryonic antigen (CEA) single-chain variable fragment (scFv) antibody MFE23 to α-sarcin, a potent fungal ribotoxin. One construct corresponds to a conventional monomeric single-chain immunotoxin design (IMTXCEAαS), while the other one takes advantage of the trimerbody technology and exhibits a novel trimeric format (IMTXTRICEAαS) with enhanced properties compared with their monomeric counterparts, including size, functional afnity and biodistribution, which endow them with an improved tumor targeting capacity. Our results show the highly specifc cytotoxic activity of both immunotoxins in vitro, which was enhanced in the trimeric format compared to the monomeric version. Moreover, the trimeric immunotoxin also exhibited superior antitumor activity in vivo in mice bearing human colorectal cancer xenografts. Therefore, trimeric immunotoxins represent a further step in the development of next-generation therapeutic immunotoxins

Pagurta: An interspecific hybrid of common seabream Pagrus pagrus (L., 1758) female and banded seabream males Pagrus auriga Valenciennes, 1843 male: phenotypic and molecular characterization

Hybrids are of great interest in aquaculture. In the present study, we report for the first time an interespecific hybrid between common seabream Pagrus pagrus (L., 1758) females and red banded seabream Pagrus auriga (Valenciennes, 1843) males, which has been named the pagurta. This hybrid was detected in natural spawns during the period from March to April 2004. Phenotipically, the hybrid possessed morphological and meristic characteristics of both parental species. Mitochondrial and nuclear (microsatellite and satellite) molecular markers were used to confirm they were hybrids. The reciprocal cross was not detected.Los híbridos suscitan gran interés en la acuicultura. Sin embargo, su aplicación industrial en espáridos ha estado limitada por las dificultades técnicas que ocasiona su desarrollo. En este trabajo se describe el nacimiento no inducido, o espontáneo, de híbridos entre pargo Pagrus pagrus (L., 1758) y hurta Pagrus auriga Valenciennes, 1843 cuando dichas especies coexisten en un mismo tanque. Estos híbridos surgieron durante los meses de marzo y abril de 2004, cuando se registraron las puestas más abundantes de ambas especies. Fenotípicamente, presentaron características propias de ambas especies parentales. La aplicación de marcadores mitocondriales y nucleares (microsatélite y satélite) permitieron confirmar que eran híbridos intergenéricos de P. pagrus (♀ ) ˟ P. auriga (♂ ) a los que se denominó pagurta. El cruce recíproco no se detectó.Instituto Español de Oceanografí

A chromosome-level genome assembly enables the identification of the follicule stimulating hormone receptor as the master sex determining gene in the flatfish Solea senegalensis

Sex determination (SD) shows huge variation among fish and a high evolutionary rate, as illustrated by the Pleuronectiformes (flatfishes). This order is characterized by its adaptation to demersal life, compact genomes and diversity of SD mechanisms. Here, we assembled the Solea senegalensis genome, a flatfish of great commercial value, into 82 contigs (614 Mb) combining long- and short-read sequencing, which were next scaffolded using a highly dense genetic map (28,838 markers, 21 linkage groups), representing 98.9% of the assembly. Further, we established the correspondence between the assembly and the 21 chromosomes by using BAC-FISH. Whole genome resequencing of six males and six females enabled the identification of 41 SNP variants in the follicle stimulating hormone receptor (fshr) consistent with an XX / XY SD system. The observed sex association was validated in a broader independent sample, providing a novel molecular sexing tool. Fshr displayed differential gene expression between male and female gonads from 86 days post-fertilization, when the gonad is still an undifferentiated primordium, concomitant with the activation of amh and cyp19a1a, testis and ovary marker genes, respectively, in males and females. The Y-linked fshr allele, which included 24 non-synonymous variants and showed a highly divergent 3D protein structure, was overexpressed in males compared to the X-linked allele at all stages of gonadal differentiation. We hypothesize a mechanism hampering the action of the follicle stimulating hormone driving the undifferentiated gonad toward testis.info:eu-repo/semantics/acceptedVersio

Assessment of parental contributions to fast- and slow-growing progenies in the sea bream Sparus aurata L. using a new multiplex PCR

Molecular tools to assist breeding programs in the gilthead sea bream (Sparus aurata L.) are scarce. A new multiplex PCR technique (OVIDORPLEX), which amplifies nine known microsatellite markers, was developed in this work. This multiplex system showed a high mean heterozygosity (>0.800) and a high mean number of alleles per marker (>14) when tested in two sea bream broodstocks (A: 40 breeders and B: 38 breeders). We tested this multiplex PCR for inferring parentage in a Spanish hatchery that graded the animals by size as part of their management procedure. The progeny of the broodstock were divided into fast- and slow-growth groups. Parentage studies revealed that this management procedure entailed a global reduction of the breeders' representation in progeny and that breeders' contributions were significantly unequal. Due to this, effective sample sizes fell to N ê¿13-14 for fast- and N ê¿18-24 for slow-growth progeny groups. These results imply a 3 to 4% rate of inbreeding per generation in the fast-growth group, which is more important to hatchery managers than the slow group. Not all the progeny were evaluated in this experiment (due to the discarding steps), and thus it is difficult to know if the phenotypic performance showed by the fast-growing progeny will be heritable. However, there were genetic differences between the differentiated growth progeny groups (fast vs. slow, F ST values=0.016 to 0.023; P<0.01). We also identified breeders with significantly different contributions to the fast- (10 breeders) or to the slow- (15 breeders) growth progeny groups. Our results demonstrated that this new multiplex PCR could be useful for quantitative programs (breeding programs, detection of QTL, inbreeding control or reconstruction of fish genealogies) to improve the aquaculture of the gilthead sea bream (S. aurata). © 2011 Elsevier B.V.This work was carried out in collaboration with the fish farm Granja Marina Safor, S.L. (Gandia, Valencia, Spain) and the hatchery Piscicultura Marina Mediterranea, S.L. (Burriana, Castellon, Spain). It was financed by JACUMAR (the PROGENSA project) and the Spanish Ministry of Science and Innovation (MICINN; National Program of Resources and Food and Agriculture Technologies, AGL2006-13411-C03-00, SELECTSPARUS, and AGL2007-64040-C03-00, SELECTBREAM, including European Regional Development Funds). V. Gallego was supported by a FPI scholarship financed by MICINN; C. Garcia-Fernandez was supported by a FPU scholarship financed by MICINN; and I. Mazzeo was supported by a FPI scholarship financed by Generalitat Valenciana. We are indebted to three anonymous referees and the journal editor for valuable comments.Borrell, YJ.; Gallego Albiach, V.; García Fernández, C.; Mazzeo ., I.; Pérez Igualada, LM.; Asturiano Nemesio, JF.; Carleos, CE.... (2011). Assessment of parental contributions to fast- and slow-growing progenies in the sea bream Sparus aurata L. using a new multiplex PCR. Aquaculture. 314(1-4):58-65. https://doi.org/10.1016/j.aquaculture.2011.01.028S58653141-