8. The leading cause of RTT is sporadic mutations in a gene called MECP2, located on the X chromosome. Studies have shown that more then 95% of mutations originate from a mutated sperm. The MECP2 gene makes a protein, also called MeCP2, believed to play a pivotal role in silencing other genes . Scientists suspect that the inability to shut down specific genes causes the cascade of symptoms seen in RTT. Methyl cytosine binding protein 2 Rett syndrome rare progressive neurological disorder that causes mental retardation, compulsive hand movements, reduced muscle tone, difficulties in walking, autism, decreased body weight, failure of the head to grow with age, and the increased presence of ammonia in the blood (hyperammonemia). Rett syndrome causes progressive disabilities in intellectual and motor development.
9.
10. Regulation of trp transcription Low tryptophane level – transcription of trp genes
11. High glucose – low cAMP Low lactose Low glucose – high cAMP Low lactose Low glucose – high cAMP High lactose High glucose – low cAMP High lactose Synthesis of LacZYA proteins: 1. Glucose level - low glucose – high cAMP 2. Lactose level - h igh lactose + - - - transcription
12. Regulation of lac transcription High glucose – low cAMP Low lactose -galactosidase permease transacetylase Low glucose – high cAMP Low lactose Low glucose – high cAMP High lactose High glucose – low cAMP High lactose CAMP receptor protein
23. MicroRNAs (miRNAs) are small, RNA molecules encoded in the genomes of plants and animals (Figure 1). These highly conserved, ~21-mer RNAs regulate the expression of genes by binding to the 3'-untranslated regions (3'-UTR) of specific mRNAs. Although the first published description of an miRNA appeared ten years ago (Lee 1993), only in the last two to three years has the breadth and diversity of this class of small, regulatory RNAs been appreciated. A great deal of effort has gone into understanding how, when, and where miRNAs are produced and function in cells, tissues, and organisms. Each miRNA is thought to regulate multiple genes , and since hundreds of miRNA genes are predicted to be present in higher eukaryotes (Lim 2003b) the potential regulatory circuitry afforded by miRNA is enormous. Several research groups have provided evidence that miRNAs may act as key regulators of processes as diverse as early development (Reinhart 2000), cell proliferation and cell death (Brennecke 2003), apoptosis and fat metabolism (Xu 2003), and cell differentiation (Dostie 2003, Chen 2003). Recent studies of miRNA expression implicate miRNAs in brain development (Krichevsky 2003), chronic lymphocytic leukemia (Calin 2002), colonic adenocarcinoma (Michael 2003), Burkitt’s Lymphoma (Metzler 2004), and viral infection (Pfeffer 2004) suggesting possible links between miRNAs and viral disease, neurodevelopment, and cancer. There is speculation that in higher eukaryotes, the role of miRNAs in regulating gene expression could be as important as that of transcription factors. Figure 1 . Transcription of miRNAs. Approximately 60% of miRNAs are expressed independently, 15% of miRNAs are expressed in clusters, and 25% are in introns.