LECTURE 5 Flashcards
How does one map a genome? (i.e. what do they use to create one)
look at genetic markers
we use maps (genetic and physical)
What is the difference between genetic maps and physical maps?
Genetic maps: look at genetic markers on chromosomes (chromosomes recombination frequency)
Physical maps: in the genome complete dna sequence (map of complete dna sequence of a genome)
Why do we complete genomic studies?
Evolutionary relationships
Genetic susceptibility to disease
Development
What is the difference between the ability to create physical genome maps now (i.e. 2022) and forty years ago?
The impossible to the easily obtainable
we can create physical genome maps faster now
The Human Genome Project began in the 1980s, what was accomplished by 1995? When was the entire genome completely sequenced?
1980’s - started
1995 - 94% of genome mapped
2003 - finished
How easy it is now to map our own individual genome?
Cost a few hundred dollars, original project was 2.7 billion dollars (cheaper now)
(its easy)
After the Human Genome Project was completed, it was found the number of genes in the human genome was _______________ genes. This represents only about 1.5 times as many genes as ______________ and nearly half as many genes as ______________. Fill in the blank.
20 thousand
fruit flies
rice
Humans, _____________, and ______________ all have about the same number of genes, it just matters how they are expressed that make us different. Fill in the blanks.
mice and puffer fishes
The Cancer Genome Project seeks the genetic basis of cancer. They have identified two categories of gene involved: oncogenes and tumor-suppressor genes. What occurs when (a) oncogenes or (b) tumor-suppressor genes mutate
oncogenes turn cancerous (gain of function)
tumor-surppressors surpress the cancer (loss of function)
Genomics have helped to fill out a cancer framework by comparing tumor genomes with the genomes of matched normal tissue. Mutations that are found in a tumor genome are divided into “driver” and “passenger” mutations. What is the difference between these two mutation types?
driver is the main reason for massive cell growth/progression of the stages within the tumor. Whereas the passenger mutations are natural and just occur whenever they want to in the tumor.
Genomes contain coding and noncoding sequences. _______________ (the intron section of DNA) constitutes around 24% of the genome (exon around 1-1.5%). Fill in the blank.
noncoding dna
Genomes contain coding and noncoding sequences. _______________ are some regions of the chromosomes which remain highly condensed, tightly coiled, and untranscribed. Fill in the blank.
structural dna
Genomes contain coding and noncoding sequences. _______________ regions tend to be localized around the centromere or near the end of the chromosome (at the telomeres). Fill in the blank.
Constitutive heterochromatin
Genomes contain coding and noncoding sequences. _______________ are scattered within the genome and are usually 1 to 5 nucleotides such as CA or CGG repeated thousands of times. Fill in the blank.
Simple sequence repeats
Genomes contain coding and noncoding sequences. _______________ are blocks of genomic sequences of 10,000 to 30,000 bp that have been duplicated and moved either within chromosomes or to a nonhomologous chromosome. Fill in the blank.
Segmental duplicants