RESUMEN
OBJECTIVE: To determine whether members of the highly phosphorylated SR protein family are autoantigens and, if so, to determine the frequency and molecular basis of antigen recognition. METHODS: Native human SR proteins were purified to homogeneity from HeLa cells, and an enzyme-linked immunosorbent assay (ELISA) was developed. Further studies employed immunoblotting of both phosphorylated and dephosphorylated SR proteins. RESULTS: Anti-SR protein reactivity was frequently detected in the sera of patients with systemic lupus erythematosus (SLE). Sera from 52% of the SLE patients in a group of patients with a variety of autoimmune and other disorders (n = 137) and from 50% of the SLE patients in a separate group (n = 102) were positive in an ELISA. In contrast, sera from patients with other disorders, such as rheumatoid arthritis and primary antiphospholipid syndrome, reacted infrequently. Reactivity with double-stranded DNA (dsDNA), used in the diagnosis of SLE, did not correlate with SR protein reactivity. Anti-SR autoantisera did not bind highly charged unphosphorylated peptides related to the SR domain, which is rich in arginine and phosphoserine residues. Surprisingly, many of the epitopes were influenced by the presence or absence of SR protein phosphorylation. In immunoblots, some patient sera lost reactivity upon SR protein dephosphorylation, while others significantly gained reactivity. CONCLUSION: We have identified a novel set of autoantigens in SLE, the SR protein family of non-small nuclear RNP pre-messenger RNA splicing factors. Anti-SR autoantibodies are distinct from those which bind dsDNA. The identification of this new set of autoantigens and the observation that the auto-epitope(s) involves posttranslational modification offer new possibilities for understanding autoimmunity and its development.
Asunto(s)
Lupus Eritematoso Sistémico/inmunología , Proteínas Nucleares/inmunología , Anticuerpos Antinucleares/sangre , Síndrome Antifosfolípido/sangre , Síndrome Antifosfolípido/inmunología , Autoantígenos/inmunología , Ensayo de Inmunoadsorción Enzimática , Epítopos/metabolismo , Células HeLa , Humanos , Inmunohistoquímica , Lupus Eritematoso Sistémico/sangre , Fosforilación , Proteínas de Unión al ARN , Factores de Empalme Serina-ArgininaRESUMEN
Although considerable information is currently available about the factors involved in constitutive vertebrate polyadenylation, the factors and mechanisms involved in facilitating communication between polyadenylation and splicing are largely unknown. Even less is known about the regulation of polyadenylation in genes in which 3'-terminal exons are alternatively recognized. Here we demonstrate that an SR protein, SRp20, affects recognition of an alternative 3'-terminal exon via an effect on the efficiency of binding of a polyadenylation factor to an alternative polyadenylation site. The gene under study codes for the peptides calcitonin and calcitonin gene-related peptide. Its pre-mRNA is alternatively processed by the tissue-specific inclusion or exclusion of an embedded 3'-terminal exon, exon 4, via factors binding to an intronic enhancer element that contains both 3' and 5' splice site consensus sequence elements. In cell types that preferentially exclude exon 4, addition of wild-type SRp20 enhances exon 4 inclusion via recognition of the intronic enhancer. In contrast, in cell types that preferentially include exon 4, addition of a mutant form of SRp20 containing the RNA-binding domain but missing the SR domain inhibits exon 4 inclusion. Inhibition is likely at the level of polyadenylation, because the mutant SRp20 inhibits binding of CstF to the exon 4 poly(A) site. This is the first demonstration that an SR protein can influence alternative polyadenylation and suggests that this family of proteins may play a role in recognition of 3'-terminal exons and perhaps in the communication between polyadenylation and splicing.
Asunto(s)
Péptido Relacionado con Gen de Calcitonina/genética , Calcitonina/genética , Elementos de Facilitación Genéticos , Precursores del ARN/metabolismo , Procesamiento Postranscripcional del ARN , Proteínas de Unión al ARN/metabolismo , Ribonucleoproteína Nuclear Pequeña U1/metabolismo , Animales , Secuencia de Bases , Calcitonina/biosíntesis , Péptido Relacionado con Gen de Calcitonina/biosíntesis , Secuencia de Consenso , Exones , Humanos , Metalotioneína/biosíntesis , Metalotioneína/genética , Ratones , Datos de Secuencia Molecular , Poli A/metabolismo , Ratas , Alineación de Secuencia , Homología de Secuencia de Ácido Nucleico , Factores de Empalme Serina-Arginina , Glándula Tiroides/metabolismo , VertebradosRESUMEN
If pre-mRNA splicing begins during RNA synthesis, then transcriptionally active genes may be expected to contain high concentrations of pre-mRNA splicing factors. However, previous studies have localized splicing factors to a network of "speckles," which is distinct from individual sites of gene transcription where pre-mRNA is spliced. Speckles have been detected with antibodies specific for splicing snRNPs and members of the SR family of splicing factors. Here we report that dilution of these probes results in the visualization of hundreds of sites throughout the HeLa cell nucleus, the size and distribution of which are consistent with transcription units viewed with light microscopy. Importantly, these sites of highest SR protein concentration frequently coincide in three-dimensional space with active sites of RNA polymerase II transcription. A newly developed reagent specific for a single member of the SR family, SRp20, detects a subset (approximately 20%) of these sites, suggesting the gene-specific accumulation of these splicing regulators, which have distinct functions in pre-mRNA splicing. These observations question the view that the nucleus and its functions are highly compartmentalized; instead, they support a model in which the localization of these and possibly other gene regulators is determined primarily by their function.
Asunto(s)
ARN Polimerasa II/genética , Precursores del ARN/metabolismo , Empalme del ARN , Anticuerpos Monoclonales , Sitios de Unión , Núcleo Celular/metabolismo , Técnica del Anticuerpo Fluorescente Indirecta , Células HeLa , Humanos , Proteínas Nucleares/inmunología , Proteínas Nucleares/metabolismo , Fosfoproteínas/inmunología , Fosfoproteínas/metabolismo , Precursores del ARN/genética , Proteínas de Unión al ARN , Ribonucleoproteínas Nucleares Pequeñas/metabolismo , Factores de Empalme Serina-Arginina , Transcripción Genética , Uridina Trifosfato/análogos & derivados , Uridina Trifosfato/metabolismoRESUMEN
The cardiac troponin T pre-mRNA contains an exonic splicing enhancer that is required for inclusion of the alternative exon 5. Here we show that enhancer activity is exquisitely sensitive to changes in the sequence of a 9-nucleotide motif (GAGGAAGAA) even when its purine content is preserved. A series of mutations that increased or decreased the level of exon inclusion in vivo were used to correlate enhancer strength with RNA-protein interactions in vitro. Analyses involving UV cross-linking and immunoprecipitation indicated that only four (SRp30a, SRp40, SRp55, and SRp75) of six essential splicing factors known as SR proteins bind to the active enhancer RNA. Moreover, purified SRp40 and SRp55 activate splicing of exon 5 when added to a splicing-deficient S100 extract. Purified SRp30b did not stimulate splicing in S100 extracts, which is consistent with its failure to bind the enhancer RNA. In vitro competition of SR protein splicing activity and UV cross-linking demonstrated that the sequence determinants for SR protein binding were precisely coincident with the sequence determinants of enhancer strength. Thus, a subset of SR proteins interacts directly with the exonic enhancer to promote inclusion of a poorly defined alternative exon. Independent regulation of the levels of SR proteins may, therefore, contribute to the developmental regulation of exon inclusion.
Asunto(s)
Empalme Alternativo , Exones/genética , Miocardio/química , Proteínas de Unión al ARN/metabolismo , Troponina/genética , Secuencia de Bases , Reactivos de Enlaces Cruzados , Células HeLa , Humanos , Datos de Secuencia Molecular , Mutación Puntual , Pruebas de Precipitina , Unión Proteica , Relación Estructura-Actividad , Fracciones Subcelulares/metabolismo , Troponina T , Rayos UltravioletaRESUMEN
The removal of introns from eukaryotic pre-mRNA occurs in a large ribonucleoprotein complex called the spliceosome. We have generated a monoclonal antibody (mAb 16H3) against four of the family of six SR proteins, known regulators of splice site selection and spliceosome assembly. In addition to the reactive SR proteins, SRp20, SRp40, SRp55, and SRp75, mAb 16H3 also binds approximately 20 distinct nuclear proteins in human, frog, and Drosophila extracts, whereas yeast do not detectably express the epitope. The antigens are shown to be nuclear, nonnucleolar, and concentrated at active sites of RNA polymerase II transcription which suggests their involvement in pre-mRNA processing. Indeed, most of the reactive proteins observed in nuclear extract are detected in spliceosomes (E and/or B complex) assembled in vitro, including the U1 70K component of the U1 small nuclear ribonucleoprotein particle and both subunits of U2AF. Interestingly, the 16H3 epitope was mapped to a 40-amino acid polypeptide composed almost exclusively of arginine alternating with glutamate and aspartate. All of the identified antigens, including the human homolog of yeast Prp22 (HRH1), contain a similar structural element characterized by arginine alternating with serine, glutamate, and/or aspartate. These results indicate that many more spliceosomal components contain such arginine-rich domains. Because it is conserved among metazoans, we propose that the "alternating arginine" domain recognized by mAb 16H3 may represent a common functional element of pre-mRNA splicing factors.
Asunto(s)
Epítopos , Proteínas Nucleares/inmunología , Empalme del ARN/inmunología , Proteínas de Unión al ARN/inmunología , Empalmosomas/inmunología , Animales , Anticuerpos Monoclonales , Especificidad de Anticuerpos , Compartimento Celular , Drosophila , Humanos , Inmunohistoquímica , Células L , Ratones , Proteínas Nucleares/aislamiento & purificación , Precursores del ARN/metabolismo , Proteínas de Unión al ARN/clasificación , Proteínas de Unión al ARN/aislamiento & purificación , Ranidae , Ribonucleoproteína Nuclear Pequeña U1RESUMEN
SR proteins are a family of proteins that have a common epitope recognized by a monoclonal antibody (MAb104) that binds active sites of polymerase II transcription. Four of the SR family members have been shown to restore activity to an otherwise splicing-deficient extract (S100 extract). Here we show that two untested SR proteins, SRp20 and SRp75, can also complement the splicing-deficient extract. We isolated a cDNA encoding SRp75 and found that this protein, like other SR proteins, contains an N-terminal RNA recognition motif (RRM), a glycine-rich region, an internal region homologous to the RRM, and a long (315-amino-acid) C-terminal domain composed predominantly of alternating serine and arginine residues. The apparent molecular mass of dephosphorylated SRp75 is 57 kDa, the size predicted from the cDNA clone. We also detected mobility shifts after dephosphorylating SRp55, SRp40, SRp30a, and SRp30b; the sizes of the shifts are proportional to the length of the SR domain, suggesting that serines in this domain are phosphorylated.
Asunto(s)
Empalme del ARN , Proteínas de Unión al ARN/genética , Secuencia de Aminoácidos , Secuencia de Bases , ADN/aislamiento & purificación , Células HeLa , Humanos , Immunoblotting , Datos de Secuencia Molecular , Fosforilación , Procesamiento Proteico-Postraduccional , ARN Polimerasa II/genética , ARN Polimerasa II/metabolismo , Proteínas de Unión al ARN/metabolismo , Factores de Empalme Serina-ArgininaRESUMEN
Alternative splicing of precursor messenger RNAs (pre-mRNAs) is a common mechanism of regulating gene expression. SR proteins are a family of pre-mRNA splicing factors that are structurally related and evolutionarily conserved. Any member of the SR family can complement a splicing-deficient extract that lacks the entire family of SR proteins. Here it is demonstrated that particular SR proteins have distinct functions in alternative pre-mRNA splicing in vitro. In addition, SR proteins are differentially expressed in a variety of tissues. These results suggest a fundamental role for SR proteins in the regulation of alternative splicing.
Asunto(s)
Empalme Alternativo , Precursores del ARN/genética , Proteínas de Unión al ARN/fisiología , Secuencia de Aminoácidos , Extractos Celulares , Células HeLa , Humanos , Datos de Secuencia Molecular , Empalme del ARN , ARN Viral/genética , Virus 40 de los Simios/genéticaRESUMEN
The adhesive interactions of circulating blood cells are tightly regulated, receptor-mediated events. To establish a model for studies on regulation of cell adhesion, we have examined the adhesive properties of the HD11 chick myeloblast cell line. Function-perturbing antibodies were used to show that integrins containing the beta 1 subunit mediate HD11 cell attachment to several distinct extracellular matrix proteins, specifically fibronectin, collagen, vitronectin, and fibrinogen. This is the first evidence that an integrin heterodimer in the beta 1 family functions as a receptor for fibrinogen. While the alpha v beta 1 heterodimer has been shown to function as a vitronectin receptor on some cells, this heterodimer could not be detected on HD11 cells. Instead, results suggest that the beta 1 subunit associates with different, unidentified alpha subunit(s) to form receptors for vitronectin and fibrinogen. Results using function-blocking antibodies also demonstrate that on these cells, additional receptors for vitronectin are formed by alpha v beta 3 and alpha v associated with an unidentified 100-kD beta subunit. The adhesive interactions of HD11 cells with these extracellular matrix ligands were shown to be regulated by lipopolysaccharide treatment, making the HD11 cell line attractive for studies of mechanisms regulating cell adhesion. In contrast to primary macrophage which rapidly exhibit enhanced adhesion to laminin and collagen upon activation, activated HD11 cells exhibited reduced adhesion to most extracellular matrix constituents.
Asunto(s)
Adhesión Celular , Fibrinógeno/metabolismo , Glicoproteínas/metabolismo , Integrinas/metabolismo , Músculos/citología , Secuencia de Aminoácidos , Animales , Línea Celular , Pollos , Datos de Secuencia Molecular , Músculos/metabolismo , Oligopéptidos/farmacología , Glicoproteínas de Membrana Plaquetaria/metabolismo , Receptores Inmunológicos/metabolismo , Receptores de Vitronectina , VitronectinaAsunto(s)
Retina/embriología , Vías Visuales/embriología , Animales , Axones/ultraestructura , Adhesión Celular/fisiología , Proteínas de la Matriz Extracelular/fisiología , Técnicas In Vitro , Integrinas/fisiología , Neuronas/citología , Neuronas/fisiología , Quiasma Óptico/embriología , Retina/citología , Retina/fisiología , Vías Visuales/citología , Vías Visuales/fisiologíaRESUMEN
Integrins are a family of alpha beta heterodimeric receptors that mediate cell-cell and cell-substratum interactions. Integrin binding to extracellular ligands regulates cell adhesion, shape, motility, intracellular signalling and gene expression. Mechanisms that regulate integrin function are, therefore, central to the participation of integrins in a diverse set of cellular events. Here we report the identification of TASC, a monoclonal antibody to a novel epitope on the integrin beta 1 subunit, which inhibits cell adhesion to vitronectin but promotes adhesion to laminin and collagen types I and IV. We show that developing retinal neurons that have lost responsiveness to laminin regain the ability to bind laminin in the presence of TASC. Thus, beta 1-class integrins are likely to occupy multiple affinity states that can be modulated at the cell surface.
Asunto(s)
Integrinas/metabolismo , Neuronas/metabolismo , Retina/citología , Secuencia de Aminoácidos , Animales , Anticuerpos Monoclonales/inmunología , Anticuerpos Monoclonales/farmacología , Bovinos , Adhesión Celular/efectos de los fármacos , Embrión de Pollo , Colágeno/metabolismo , Epítopos/inmunología , Glicoproteínas/metabolismo , Immunoblotting , Integrinas/inmunología , Laminina/metabolismo , Datos de Secuencia Molecular , Peso Molecular , Fragmentos de Péptidos/farmacología , Retina/embriología , VitronectinaRESUMEN
Extracellular matrix (ECM) glycoproteins regulate neuronal development and axonal growth. In this paper, the ECM glycoprotein vitronectin was identified and localized in the embryonic chick neuroretina. To identify potentially important neurite outgrowth-promoting molecules, responses of embryonic chick retinal neurons to vitronectin and thrombospondin, another retinal ECM constituent, were examined. These neurons were shown to attach and extend neurites on either glycoprotein. Integrins containing the alpha v or beta 1 subunits mediate both responses to vitronectin and neurite outgrowth on thrombospondin. Attachment to thrombospondin was inhibited by heparin, suggesting that neurons also utilize a proteoglycan or sulfated glycolipid as a receptor for this glycoprotein. Thus, retinal neurons use specific receptors to interact with vitronectin and thrombospondin, two glycoproteins present in the embryonic neuroretina, suggesting roles for these ligands and their receptors in retinal development.
Asunto(s)
Axones/fisiología , Glicoproteínas/fisiología , Integrinas/fisiología , Glicoproteínas de Membrana Plaquetaria/fisiología , Retina/fisiología , Animales , Axones/efectos de los fármacos , Axones/ultraestructura , Antígenos CD36 , Embrión de Pollo , Glucolípidos/fisiología , Glicoproteínas/metabolismo , Heparina/farmacología , Histocitoquímica/métodos , Immunoblotting , Glicoproteínas de Membrana Plaquetaria/metabolismo , Pruebas de Precipitina , Proteoglicanos/fisiología , Receptores de Citoadhesina/efectos de los fármacos , Receptores de Citoadhesina/metabolismo , Receptores de Citoadhesina/fisiología , Receptores Inmunológicos/efectos de los fármacos , Receptores Inmunológicos/metabolismo , Receptores Inmunológicos/fisiología , Receptores de Vitronectina , Retina/embriología , Retina/metabolismo , Trombospondinas , VitronectinaAsunto(s)
Axones/fisiología , Moléculas de Adhesión Celular/fisiología , Matriz Extracelular/metabolismo , Integrinas/fisiología , Receptores de Neurotransmisores/fisiología , Animales , Axones/efectos de los fármacos , Moléculas de Adhesión Celular/metabolismo , Diferenciación Celular , Integrinas/metabolismo , Receptores de Neurotransmisores/metabolismoRESUMEN
Retinal ganglion neurons extend axons that grow along astroglial cell surfaces in the developing optic pathway. To identify the molecules that may mediate axon extension in vivo, antibodies to neuronal cell surface proteins were tested for their effects on neurite outgrowth by embryonic chick retinal neurons cultured on astrocyte monolayers. Neurite outgrowth by retinal neurons from embryonic day 7 (E7) and E11 chick embryos depended on the function of a calcium-dependent cell adhesion molecule (N-cadherin) and beta 1-class integrin extracellular matrix receptors. The inhibitory effects of either antibody on process extension could not be accounted for by a reduction in the attachment of neurons to astrocytes. The role of a third cell adhesion molecule, NCAM, changed during development. Anti-NCAM had no detectable inhibitory effects on neurite outgrowth by E7 retinal neurons. In contrast, E11 retinal neurite outgrowth was strongly dependent on NCAM function. Thus, N-cadherin, integrins, and NCAM are likely to regulate axon extension in the optic pathway, and their relative importance varies with developmental age.
Asunto(s)
Antígenos de Superficie , Astrocitos/fisiología , Axones/fisiología , Glicoproteínas de Membrana/fisiología , Retina/fisiología , Células Ganglionares de la Retina/fisiología , Animales , Anticuerpos Monoclonales/inmunología , Antígenos de Superficie/inmunología , Adhesión Celular , Moléculas de Adhesión Celular , Células Cultivadas , Embrión de Pollo , Integrinas , Laminina/metabolismo , Glicoproteínas de Membrana/inmunología , Ratones , Ratas , Receptores Inmunológicos/metabolismo , Especificidad por SustratoRESUMEN
Receptor-mediated interactions between neurons and astroglia are likely to play a crucial role in the growth and guidance of CNS axons. Using antibodies to neuronal cell surface proteins, we identified two receptor systems mediating neurite outgrowth on cultured astrocytes. N-cadherin, a Ca2(+)-dependent cell adhesion molecule, functions prominently in the outgrowth of neurites on astrocytes by E8 and E14 chick ciliary ganglion (CG) neurons. beta 1-class integrin ECM receptor heterodimers function less prominently in E8 and not at all in E14 neurite outgrowth on astrocytes. The lack of effect of integrin beta 1 antibodies on E14 neurite outgrowth reflects an apparent loss of integrin function, as assayed by E14 neuronal attachment and process outgrowth on laminin. N-CAM appeared not to be required for neurite outgrowth by either E8 or E14 neurons. Since N-cadherin and integrin beta 1 antibodies together virtually eliminated E8 CG neurite outgrowth on cultured astrocytes, these two neuronal receptors are probably important in regulating axon growth on astroglia in vivo.
Asunto(s)
Astrocitos/citología , Cadherinas/fisiología , Integrinas/fisiología , Factores de Crecimiento Nervioso/fisiología , Receptores de Superficie Celular/metabolismo , Animales , Astrocitos/efectos de los fármacos , Astrocitos/metabolismo , Cadherinas/inmunología , Corteza Cerebral/citología , Corteza Cerebral/efectos de los fármacos , Pollos , Dendritas/efectos de los fármacos , Ganglios Parasimpáticos/citología , Ganglios Parasimpáticos/efectos de los fármacos , Sueros Inmunes/farmacología , Integrinas/inmunología , Factores de Crecimiento Nervioso/inmunología , Factores de Crecimiento Nervioso/farmacología , Ratas , Ratas Endogámicas , Receptores de Superficie Celular/inmunología , Receptores de Factor de Crecimiento NerviosoRESUMEN
Cell attachment and neurite outgrowth by embryonic neural retinal cells were measured in separate quantitative assays to define differences in substrate preference and to demonstrate developmentally regulated changes in cellular response to different extracellular matrix glycoproteins. Cells attached to laminin, fibronectin, and collagen IV in a concentration-dependent fashion, though fibronectin was less effective for attachment than the other two substrates. Neurite outgrowth was much more extensive on laminin than on fibronectin or collagen IV. These results suggest that different substrates have distinct effects on neuronal differentiation. Neural retinal cell attachment and neurite outgrowth were inhibited on all three substrates by two antibodies, cell substratum attachment antibody (CSAT) and JG22, which recognize a cell surface glycoprotein complex required for cell interactions with several extracellular matrix constituents. In addition, retinal cells grew neurites on substrates coated with the CSAT antibodies. These results suggest that cell surface molecules recognized by this antibody are directly involved in cell attachment and neurite extension. Neural retinal cells from embryos of different ages varied in their capacity to interact with extracellular matrix substrates. Cells of all ages, embryonic day 6 (E6) to E12, attached to collagen IV and CSAT antibody substrates. In contrast, cell attachment to laminin and fibronectin diminished with increasing embryonic age. Age-dependent differences were found in the profile of proteins precipitated by the CSAT antibody, raising the possibility that modifications of these proteins are responsible for the dramatic changes in substrate preference of retinal cells between E6 and E12.