Biochem 432: Genetics Flashcards
Genes and structure, chromosomes, genomics and computational methods (lecture 16) Final Exam
Describe the two types of sequence organization for prokaryotic genes
- Monocistronic prokaryotic genes encode one protein product in a single RNA transcript.
- Polycistronic prokaryotic genes encode multiple protein products in a single RNA transcript. Polycistronic genes are not organized at random; their gene products frequently have a related function or are part of a regulatory unit in the cell.
Describe the typicaly eukaryotic gene organization
The structure of a eukaryotic gene contains the upstream regulatory sequences and the promoter sequences, as well as the 5’-UTR upstream of the coding sequence.
The precursor RNA transcript contains the intron and exon sequences, as well as the 5’-UTR and 3’-UTR.
Concurrent with synthesis of the precursor mRNA by RNA polymerase, the transcript undergoes RNA processing to remove intron sequences, add a 5’-cap, and add a 3’-poly(A) tail before being exported from the nucleus to the cytoplasm.
Exons are coding regions and introns are noncoding regions that must be removed.
UTR – untranslated region.
Explain the concept of chromosomes
Chromosomes are thread-like structures located inside the nucleus of animal and plant cells during mitosis.
Each chromosome is made of protein and a single molecule of deoxyribonucleic acid (DNA).
Passed from parents to offspring, DNA contains the specific instructions that make each type of living creature unique.
In humans, each cell normally contains 23 pairs of chromosomes, for a total of 46
Overview the cell cycle meiosis (how chromosomes split into daughter cells)
G0: Nondividing state
G1, S, G2: Dividng cells have mitosis pahse and interpahse (chromosomes are amorphus and dispersed)
Prophase of mitosis: chromosomes are condensed and sister chromatid pairs are formed
Describe centromeres
Region where the two daughter chromosomes are held together during mitosis
—- after DNA replication but before cell division
Essential for equal distribution of chromosome sets to daughter cells
Link the chromosome to the mitotic spindle
Have AT-rich repeated sequences of ~130 bp
Overview meiosis, focusing on what happens between homologous chromosomes
Meiosis I: crossover can occur between homologous chromosomes (recombination)
Meiosis II: separation of homologs into haploid cells
What’s the difference between haploid and diploid cells?
Haploid:
Cells with one set of chromosome, e.g. gametes (23 in human cells)
Diploid:
Cells have two sets of chromosomes (23 pairs with 46 in total in human cells)
Why is condensation of eukaryotic DNA usefule?
Condensation of eukaryotic DNA into chromosomes reduces the size of the DNA. The assembly of nucleosomes facilitates the tight compaction of mitotic chromosomes.
Explain post-translational modifications observed on human histones
Modifications of histone tails by acetylation, methylation, phosphorylation, and ubiquitinylation control chromatin condensation and function.
Histones in a single nucleosome usually contain several, but not all, tail modifications simultaneously.
Histone code: specific post-transcriptional modification combinations in different chromatin regions specifically influence chromatin function by creating or removing chromatin-associated protein binding sites.
Describe nucleosomes
Nucleosomes consist of DNA wrapped around histones
Amino-terminal tails of histones stick out, form sites for covalent modification, and form important contacts between nucleosomes.
Covalent modifications of the histones and DNA by cellular enzymes influence whether the DNA is in the more condensed form or not.
What’s the difference between euchromatin and heterochromatin?
euchromatin – light-staining, whitish areas – includes most transcribed regions
heterochromatin – dark-staining – includes centromeres, telomeres, and transcriptionally inactive genes
Histone modifications play integral roles in chromatin condensation and function. Which of the following is NOT considered to be a histone modification?
- acetylation
- methylation
- phosphorylation
Prenylation is a common lipid modification
What is/are true about Philadelphia chromosome
- can be detected by chromosome painting
- involves translocation between the long arm of chromosome 9 and long arm of chromosome 22
- involves translocation between the long arm of chromosome 9 and short arm of chromosome 21
- can be found in chronic myelogenous leukemia
- can be detected by chromosome painting
- involves translocation between the long arm of chromosome 9 and long arm of chromosome 22
- can be found in chronic myelogenous leukemia