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Text S1.
Text S1.

... bp from both transposon termini. Each tRNALys gene can be transcribed but does not encode a functional product. Upon insertion, the element generates a 9-bp target site duplication (TSD), which is characteristic for Mu-like elements. Based on EST evidence, two transcripts stem from the presumptive a ...
Dosage Compensation: Transcription-Level Regulation of X
Dosage Compensation: Transcription-Level Regulation of X

... Drosophila, it is not surprising that gene activity of X and autosome segments is autonomous in translocations: X-linked genes are subjected to dosage compensation even when they are relocated elsewhere in the genome; autosomal genes transposed to the X do not become dosage compensated. An example o ...
The Genetics and Molecular Biology of Huntington*s Disease
The Genetics and Molecular Biology of Huntington*s Disease

... Molecular Biology of HD-Background *Exon 1 of the HD gene contains a segment of uninterrupted CAG trinucleotide repeats, which is translated into a polyglutamine tract in the huntingtin protein. -mouse studies have shown that CAG/polyglutamine mutations lead to deleterious functions on mutant HD pr ...
This lecture: parts of Ch 16/26: Population
This lecture: parts of Ch 16/26: Population

... selection weeds out most deleterious alleles, leaving those that best suit organisms to their environments. • Mutations are likely to be beneficial when the relationship of the organism to its environment changes; organism is pre-adapted to change. • Selection for beneficial mutations is the basis f ...
Exam 2 Key
Exam 2 Key

... a. will be passed on to all of his children b. will be passed on to all of his sons, but none of his daughters c. will be passed on to all of his sons, and half of his daughters d. will be passed on to half his sons, but none of his daughters e. *will not be passed on to any of his children 3. The l ...
Describe the central dogma of molecular biology.
Describe the central dogma of molecular biology.

... Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. ...
Chapter 12: Inheritance Patterns and Human Genetics
Chapter 12: Inheritance Patterns and Human Genetics

... – Pairs of genes that tend to be inherited together are called linked genes. ...
Gene Section PTCH (patched homolog) Atlas of Genetics and Cytogenetics
Gene Section PTCH (patched homolog) Atlas of Genetics and Cytogenetics

Transcription factors - introduction
Transcription factors - introduction

... – introns are spliced out by the spliceosome, a large complex of RNA and proteins. • exons can also be spliced out as well. Alternative splicing may produce proteins with new functions. – Molecular mechanisms underlying alternative splicing are still only poorly understood – regulation of alternativ ...
DNA Technology - Biology Junction
DNA Technology - Biology Junction

... Biology, Seventh Edition ...
genes
genes

... • PUNNETT SQUARE – diagram showing the gene combinations that might result from a genetic cross • HOMOZYGOUS= The pair of alleles or genotype are identical – TT or tt • HETEROZYGOUS= The pair of alleles or genotype are different – Tt • PHENOTYPE=The way an organisms traits are expressed, physical ap ...
Basic Genetics Concepts
Basic Genetics Concepts

... several or many genes. Some genes can tolerate aneuploidy, while others are very sensitive to it. • The chromosome breaks themselves can cause genetic harm, if they break a gene in half. Otherwise, any genetic harm is due to aneuploidy. • Most of the time, a person is heterozygous for the unusual ch ...
Chp 18 Viruses and Bacteria
Chp 18 Viruses and Bacteria

... DNA is chemically altered, so it is not destroyed by the cell's own restriction enzymes. Restriction enzymes = Naturally occurring bacterial enzymes that protect bacteria against intruding DNA from other organisms. The enzymes also catalyze restriction, the process of cutting foreign DNA into small ...
BMC Genomics - LCBB
BMC Genomics - LCBB

... changes but also events that alter the chromosome structure, such as inversions, duplications or deletions [1]. Ancestral gene sequence inference has led to significant predictions of protein functional shift and positive selection [2]. For example, comparisons of orthologous chromosomal segments sh ...
Global Agenda Council on Genetics
Global Agenda Council on Genetics

... A gene commonly refers to a fundamental unit of inheritance. It resides in a stretch of DNA or RNA that can code for an RNA molecule, leading to substances – mainly proteins – that have many functions in an organism. To study genes, researchers use a process called sequencing. This process begins wi ...
ADDRESSING THE BITTER TRAIT IN CHICORY “PUNTARELLE
ADDRESSING THE BITTER TRAIT IN CHICORY “PUNTARELLE

... vegetable; Molfettese and Galatina are Apulian landraces consumed for their tender stems (turions or "puntarelle"). Bitterness is an important organoleptic trait, which directs both consumer and breeding choices and is linked to the content of sesquiterpene lactones (STLs). Major STLs (lactucin, 8-d ...
8.7 Mutations - Perry Local Schools
8.7 Mutations - Perry Local Schools

... 4. Nondisjunction – failure of homologous chromosomes to separate properly during meiosis Two possible outcomes: 1. One gamete - an extra chromosome • when fertilized - 3 copies of chromosome • trisomy 2. One gamete - one less chromosome • when fertilized - 1 copy of chromosome • monosomy ...
Developing codominant PCR markers in pines
Developing codominant PCR markers in pines

... dideoxy sequencing methods). Nucleotide sequences were then compared against published sequences contained in the GenBank electronic database to determine whether they appeared similar to any previously characterized sequences. If a tentative identification was made, then additional information was ...
Uses of heritability
Uses of heritability

... fraternal twins share environments to the same extent. Do you think this is true? a) Identical twins share embryonic ...
Chromosomal Theory of Inheritance brief notes
Chromosomal Theory of Inheritance brief notes

measuring behavior – variation
measuring behavior – variation

...  paired light & dark stimuli (A)  train: food reward for turning  right if top lighter  left if top darker  test: previously unseen pairs  able to transfer the “rule” to new situations  did not simply learn pattern of cards  learned that relationship between stimuli is critial p.12 fig.1.5 ...
Suggested Project for LEADHER program Name Fadel A. Sharif
Suggested Project for LEADHER program Name Fadel A. Sharif

... The project results will reveal the genetic causes of many childhood congenital malformations and that is of utmost importance for genetic counseling and future prenatal and preimplantation genetic testing. ...
Microviridae goes temperate: microvirus-related - HAL
Microviridae goes temperate: microvirus-related - HAL

... the presence of dif-like sequences, similar to those found in BMV1. Indeed, such sequences turned out not to be specific to BMV1, but could also be identified in BMV3–6 (Fig. 2), but not in BMV2 and BMV7. It should be noted, however, that BMV7 sequence is only partial, present on the extremity of a ...
Genetics II
Genetics II

... • The closer together two genes are, the more likely they will be inherited together. • Cross-over frequencies are related to distances between genes. ...
Lecture 4 Genome_Organization
Lecture 4 Genome_Organization

... They contain internal promoters for RNA polymerase 3. Several families, some originated as tRNA genes and others as 7SL RNA, the RNA involved in the signal recognition particle that guides secreted and membrane protein translation into the endoplasmic reticulum. – Most important SINE is the Alu sequ ...
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Site-specific recombinase technology



Nearly every human gene has a counterpart in the mouse (regardless of the fact that a minor set of orthologues had to follow species specific selection routes). This made the mouse the major model for elucidating the ways in which our genetic material encodes information. In the late 1980s gene targeting in murine embryonic stem (ES-)cells enabled the transmission of mutations into the mouse germ line and emerged as a novel option to study the genetic basis of regulatory networks as they exist in the genome. Still, classical gene targeting proved to be limited in several ways as gene functions became irreversibly destroyed by the marker gene that had to be introduced for selecting recombinant ES cells. These early steps led to animals in which the mutation was present in all cells of the body from the beginning leading to complex phenotypes and/or early lethality. There was a clear need for methods to restrict these mutations to specific points in development and specific cell types. This dream became reality when groups in the USA were able to introduce bacteriophage and yeast-derived site-specific recombination (SSR-) systems into mammalian cells as well as into the mouse
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