The SR protein family of splicing factors: master regulators of gene expression
JC Long, JF Caceres - Biochemical Journal, 2009 - portlandpress.com
The SR protein family comprises a number of phylogenetically conserved and structurally
related proteins with a characteristic domain rich in arginine and serine residues, known as …
related proteins with a characteristic domain rich in arginine and serine residues, known as …
Sorting out the complexity of SR protein functions
BR Graveley - Rna, 2000 - cambridge.org
Members of the serine/arginine-rich (SR) protein family have multiple functions in the pre-
mRNA splicing reaction. In addition to being required for the removal of constitutively spliced …
mRNA splicing reaction. In addition to being required for the removal of constitutively spliced …
The gene csd is the primary signal for sexual development in the honeybee and encodes an SR-type protein
Haplodiploid organisms comprise about 20% of animals. Males develop from unfertilized
eggs while females are derived from fertilized eggs. The underlying mechanisms of sex …
eggs while females are derived from fertilized eggs. The underlying mechanisms of sex …
Control of male sexual behavior and sexual orientation in Drosophila by the fruitless gene
LC Ryner, SF Goodwin, DH Castrillon, A Anand… - Cell, 1996 - cell.com
Sexual orientation and courtship behavior in Drosophila are regulated by fruitless (fru), the
first gene in a branch of the sex-determination hierarchy functioning specifically in the …
first gene in a branch of the sex-determination hierarchy functioning specifically in the …
Alternative splicing of pre-mRNA: developmental consequences and mechanisms of regulation
AJ Lopez - Annual review of genetics, 1998 - annualreviews.org
▪ Abstract Alternative splicing of pre-mRNAs is a powerful and versatile regulatory
mechanism that can effect quantitative control of gene expression and functional …
mechanism that can effect quantitative control of gene expression and functional …
Htra2-β1 stimulates an exonic splicing enhancer and can restore full-length SMN expression to survival motor neuron 2 (SMN2)
Y Hofmann, CL Lorson, S Stamm… - Proceedings of the …, 2000 - National Acad Sciences
Spinal muscular atrophy (SMA), a common motor neuron disease in humans, results from
loss of functional survival motor neuron (SMN1) alleles. A nearly identical copy of the gene …
loss of functional survival motor neuron (SMN1) alleles. A nearly identical copy of the gene …
Structure, function and evolution of sex-determining systems in Dipteran insects
C Schütt, R Nöthiger - Development, 2000 - journals.biologists.com
Nature has evolved an astonishing variety of genetic and epigenetic sex-determining
systems which all achieve the same result, the generation of two sexes. Genetic and …
systems which all achieve the same result, the generation of two sexes. Genetic and …
The evolutionary dynamics of sex determination
I Marın, BS Baker - Science, 1998 - science.org
REVIEW There is substantial cytogenetic data indicating that the process of sex
determination can evolve relatively rapidly. However, recent molecular studies on the …
determination can evolve relatively rapidly. However, recent molecular studies on the …
Establishing sexual dimorphism: conservation amidst diversity?
D Zarkower - Nature Reviews Genetics, 2001 - nature.com
The molecular mechanisms that control sexual dimorphism are very different in distantly
related animals. Did sex determination arise several times with different regulatory …
related animals. Did sex determination arise several times with different regulatory …
Capping, splicing, and 3′ processing are independently stimulated by RNA polymerase II: different functions for different segments of the CTD
N Fong, DL Bentley - Genes & development, 2001 - genesdev.cshlp.org
Capping, splicing, and cleavage/polyadenylation of pre-mRNAs are interdependent events
that are all stimulated in vivo by the carboxy-terminal domain (CTD) of RNA Pol II. We show …
that are all stimulated in vivo by the carboxy-terminal domain (CTD) of RNA Pol II. We show …