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vi CONTENTS
3.5 Organelle Genes: Inheritance Independent F plasmids that carry genomic fragments 188
of the Nucleus 110 R plasmids 188
Patterns of inheritance in organelles 111 5.3 Bacterial Transformation 191
Cytoplasmic segregation 113 The nature of transformation 191
Cytoplasmic mutations in humans 115 Chromosome mapping using transformation 191
mtDNA in evolutionary studies 116 5.4 Bacteriophage Genetics 192
Infection of bacteria by phages 192
4 Mapping Eukaryote Chromosomes Mapping phage chromosomes by using phage
by Recombination 127 crosses 194
4.1 Diagnostics of Linkage 129 5.5 Transduction 196
Using recombinant frequency to recognize linkage 129 Discovery of transduction 196
How crossovers produce recombinants for linked Generalized transduction 197
genes 132 Specialized transduction 198
Linkage symbolism and terminology 132 Mechanism of specialized transduction 200
Evidence that crossing over is a breakage-and-
rejoining process 133 5.6 Physical Maps and Linkage Maps Compared 201
Evidence that crossing over takes place at
the four-chromatid stage 133 6 Gene Interaction 215
Multiple crossovers can include more than two 6.1 Interactions Between the Alleles of a
chromatids 134 Single Gene: Variations on Dominance 216
4.2 Mapping by Recombinant Frequency 135 Complete dominance and recessiveness 216
Map units 136 Incomplete dominance 218
Three-point testcross 139 Codominance 219
Deducing gene order by inspection 141 Recessive lethal alleles 220
CONTENTS vii
6.2 Interaction of Genes in Pathways 223 Small nuclear RNAs (snRNAs): the mechanism
of exon splicing 307
Biosynthetic pathways in Neurospora 224
Self-splicing introns and the RNA world 308
Gene interaction in other types of pathways 226
8.5 Small Functional RNAs That Regulate
6.3 Inferring Gene Interactions 227
and Protect the Eukaryotic Genome 310
Sorting mutants using the complementation test 227
miRNAs are important regulators of gene expression 310
Analyzing double mutants of random mutations 231
siRNAs ensure genome stability 311
6.4 Penetrance and Expressivity 239 Similar mechanisms generate siRNA and miRNA 314
10.5 Aligning Genetic and Physical Maps to Gal4 regulates multiple genes through upstream
Isolate Specific Genes 377 activation sequences 436
Using positional cloning to identify a human-disease The Gal4 protein has separable DNA-binding
gene 378 and activation domains 438
Using fine mapping to identify genes 379 Gal4 activity is physiologically regulated 439
Gal4 functions in most eukaryotes 439
10.6 Genetic Engineering 382
Activators recruit the transcriptional machinery 440
Genetic engineering in Saccharomyces cerevisiae 383
The control of yeast mating type: combinatorial
Genetic engineering in plants 383 interactions 440
Genetic engineering in animals 386 12.3 Dynamic Chromatin 443
Chromatin-remodeling proteins and gene activation 444
11 Regulation of Gene Expression Modification of histones 445
in Bacteria and Their Viruses 397 Histone methylation can activate or repress
11.1 Gene Regulation 399 gene expression 448
The basics of prokaryotic transcriptional The inheritance of histone modifications and
regulation: genetic switches 400 chromatin structure 448
A first look at the lac regulatory circuit 401 Histone variants 449
11.2 Discovery of the lac System: Negative Control 404 DNA methylation: another heritable mark that
influences chromatin structure 449
Genes controlled together 405
12.4 Activation of Genes in a Chromatin
Genetic evidence for the operator and repressor 405
Environment 450
Genetic evidence for allostery 407
The β-interferon enhanceosome 451
Genetic analysis of the lac promoter 408
Enhancer-blocking insulators 452
Molecular characterization of the Lac repressor
and the lac operator 408 12.5 Long-Term Inactivation of Genes in a
Genetic analysis of the lac promoter 408 Chromatin Environment 454
Molecular characterization of the Lac repressor Mating-type switching and gene silencing 454
and the lac operator 408 Heterochromatin and euchromatin compared 455
11.3 Catabolite Repression of the lac Operon: Position-effect variegation in Drosophila reveals
Positive Control 409 genomic neighborhoods 456
Genetic analysis of PEV reveals proteins necessary
The basics of lac catabolite repression:
for heterochromatin formation 457
choosing the best sugar to metabolize 410
The structures of target DNA sites 410 12.6 Gender-Specific Silencing of Genes
and Whole Chromosomes 460
A summary of the lac operon 411
Genomic imprinting explains some unusual
11.4 Dual Positive and Negative Control:
patterns of inheritance 460
The Arabinose Operon 413
But what about Dolly and other cloned mammals? 461
11.5 Metabolic Pathways and Additional
Silencing an entire chromosome: X-chromosome
Levels of Regulation: Attenuation 414 inactivation 462
11.6 Bacteriophage Life Cycles: More 12.7 Post-Transcriptional Gene Repression
Regulators, Complex Operons 417 by miRNAs 463
Molecular anatomy of the genetic switch 421
Sequence-specific binding of regulatory proteins 13 The Genetic Control of Development 469
to DNA 422
11.7 Alternative Sigma Factors Regulate Large 13.1 The Genetic Approach to Development 471
Sets of Genes 423 13.2 The Genetic Toolkit for Drosophila
Development 474
Classification of genes by developmental function 474
12 Regulation of Gene Expression
Homeotic genes and segmental identity 474
in Eukaryotes 431
Organization and expression of Hox genes 476
12.1 Transcriptional Regulation in Eukaryotes:
The homeobox 478
An Overview 432
Clusters of Hox genes control development in
12.2 Lessons from Yeast: The GAL System 436 most animals 479
CONTENTS ix
13.3 Defining the Entire Toolkit 482 14.7 Functional Genomics and Reverse
The anteroposterior and dorsoventral axes 483 Genetics 536
Expression of toolkit genes 484 “’Omics” 536
Turning sequence reads into an assembled sequence 511 Transposable elements in the human genome 568
16.3 The Molecular Basis of Induced Mutations 593 The inbreeding coefficient 680
Mechanisms of mutagenesis 593 Population size and inbreeding 682
The Ames test: evaluating mutagens in our 18.4 Genetic Variation and Its Measurement 684
environment 595
18.5 The Modulation of Genetic Variation 687
16.4 Biological Repair Mechanisms 596
New alleles enter the population: mutation and
Direct reversal of damaged DNA 597 migration 687
Base-excision repair 598 Recombination and linkage disequilibrium 689
Nucleotide-excision repair 599 Genetic drift and population size 691
Postreplication repair: mismatch repair 602 Selection 696
Error-prone repair: translesion DNA synthesis 604 Forms of selection 698
Repair of double-strand breaks 606 Balance between mutation and drift 702
The involvement of DSB repair in meiotic Balance between mutation and selection 703
recombination 608
18.6 Biological and Social Applications 704
16.5 Cancer: An Important Phenotypic
Conservation genetics 704
Consequence of Mutation 609
Calculating disease risks 705
How cancer cells differ from normal cells 609
DNA forensics 706
Mutations in cancer cells 609
Googling your DNA mates 707
S
ince its first edition in 1974, Introduction to Genetic Analysis has emphasized
the power and incisiveness of the genetic approach in biological research
and its applications. Over its many editions, the text has continuously ex-
panded its coverage as the power of traditional genetic analysis has been extended
with the introduction of recombinant DNA technology and then genomics. In the
eleventh edition, we continue this tradition and show how the flowering of this
powerful type of analysis has been used for insight into research in biology, agri-
culture, and human health.
Pedagogical Tools
One of the important new features in this edition is the inclusion of
lists of learning outcomes at the beginning of each chapter. Learning LEARNING OUTCOMES
outcomes are crucial components of understanding. One of the tenets After completing this chapter, you will be able to
of the constructivist theory of learning is that although understand- • Perform a quantitative analysis of the
ing might be a series of new mental circuits, the learner can never be progeny of a dihybrid testcross to assess
sure of what is in his or her brain until called upon for some type of whether or not the two genes are linked on
performance. Indeed, understanding has even been defined by some the same chromosome.
as flexible performance capacity. The lists of goals show learners what • Extend the same type of analysis to several
precise performances are expected of them. The notes that follow loci to produce a map of the relative positions
of loci on a chromosome.
show how the benefits of the learning outcomes in this book can be
maximized for instructors who wish to use them. • In ascomycete fungi, map the centromeres
to other linked loci.
Classroom sessions large and small (for example, lectures and
tutorials) should be structured as far as possible on learning out- • In asci, predict allele ratios stemming from
specific steps in the heteroduplex model of
comes closely paralleling those in these chapters. At various stages crossing over.
in the classes students should be asked to demonstrate their under-
standing of the material just covered by attaining one or more learn-
ing outcomes. In writing examination or test questions, the instructor should try
to stick closely to learning outcomes. When reviewing test results, show in what
ways the outcomes have been attained or not attained by the learner.
Students should read the list of learning outcomes before embarking on a
chapter. Although it will not be possible to understand most of them before read-
ing the chapter, their wording gives a good idea of the lay of the land, and shows
the extent of what the instructor’s expectations are. Ideally, after reading a sec-
tion of the chapter, it is a good idea for a student to go back to the list and match
the material covered to an outcome. This process should be repeated at the end
of the chapter by scanning the sections and making a complete match with each
outcome as far as possible. In solving the end-of-chapter problems, try to focus
effort on the skills described in the learning outcomes. Students should use the
learning outcomes for rapid review when studying for exams; they should try to
imagine ways that they will be expected to demonstrate understanding through
the application of the outcomes.
The general goal of a course in genetics is to learn how to think and work like a
geneticist. The learning outcomes can fractionate this general goal into the many
different skills required in this analytical subject.
In this edition we have replaced “Messages” with “Key Concepts.” Messages
have been in the book since its first edition in 1974. In the 1960s and 1970s, per-
haps due to the popularity of Marshall McLuhan’s principle “The medium is the
message,” the word message was in common use, and teachers were often asked,
“What is your message?” Although with the rise of electronic media it is perhaps
time for a resurgence of McLuhan’s principle, we felt that the word message no
longer has the meaning it had in 1974.
xiii
xiv PREFACE
Flood-intolerant and flood-tolerant rice SUB1 gene increases rice yield under flooding
6.0
5.0
4.0
Yield (t ha–1)
3.0
2.0
Swarna
1.0
Swarna-Sub1
0.0
0 5 10 15 20 25 30
Duration of submergence (days)
M
A
A A H4 H3
Genome surveillance: Cutting-edge research in trans- Ser
A Lys
Lys
M A A
A
M
Lys Lys A A
posable elements has uncovered genome surveillance Lys
Ser Lys
Lys
Lys
Lys
Ser Lys
systems in plants, animals, and bacteria similar to that
previously identified in C. elegans. Chapter 15 now pro-
F igure 12 -13 (a) Histone tails protrude from the nucleosome core (purple).
vides an overview of piRNAs in animals and crRNAs in (b) Examples of histone tail modifications are shown. Circles with A represent
bacteria, and allows students to compare and contrast acetylation while circles with M represent methylation. See text for details.
those approaches to Tc1 elements in worms and MITEs in
plants.
Transcription Transcription
Inactive element
not transcribed
Processing Processing
piRNA mRNA
piwi-
Argonaute Translation
Enduring Features
Coverage of model organisms
The eleventh edition retains the enhanced coverage of model systems in formats
that are practical and flexible for both students and instructors.
• Chapter 1 introduces some key genetic model organisms and highlights some of
the successes achieved through their use.
• Model Organism boxes presented in context where appropriate provide
additional information about the organism in nature and its use experimentally.
• A Brief Guide to Model Organisms, at the back of the book, provides quick
access to essential, practical information about the uses of specific model
organisms in research studies.
• An Index to Model Organisms, on the endpapers at the back of the book,
provides chapter-by-chapter page references to discussions of specific
organisms in the text, enabling instructors and students to easily find and
assemble comparative information across organisms.
Problem sets
No matter how clear the exposition, deep understanding requires the student to
personally engage with the material. Hence our efforts to encourage student prob-
lem solving. Building on its focus on genetic analysis, the eleventh edition provides
students with opportunities to practice problem-solving skills—both in the text and
online through the following features.
• Versatile Problem Sets. Problems span the full range of degrees of
difficulty. They are categorized according to level of difficulty—basic or
challenging.
• Working with the Figures. An innovative set of problems included at the
back of each chapter asks students pointed questions about figures in the
chapter. These questions encourage students to think about the figures and
help them to assess their understanding of key concepts.
• Solved Problems. Found at the end of each chapter, these worked examples
illustrate how geneticists apply principles to experimental data.
• Unpacking the Problems. A genetics problem draws on a complex matrix
of concepts and information. “Unpacking the Problem” helps students learn
to approach problem solving strategically, one step at a time, concept on
concept.
• NEW Multiple-choice versions of the end-of-chapter
problems are available on our online LaunchPad for quick gradable quizzing
and easily gradable homework assignments. The Unpacking the Problem
tutorials from the text have been converted to in-depth online tutorials and
expanded to help students learn to solve problems and think like a geneticist.
New videos demonstrate how to solve selected difficult problems.
Includes all the electronic resources listed below for teachers. Contact your W. H.
Freeman sales representative to learn how to log on as an instructor.
e-Book
The e-Book fully integrates the text and its interactive media in a format that features
a variety of helpful study tools (full-text, Google-style searching; note taking; book-
marking; highlighting; and more). Available as a stand-alone item or on the LaunchPad.
Clicker Questions
Jump-start discussions, illuminate important points, and promote better conceptual
understanding during lectures.
Layered PowerPoint Presentations
Illuminate challenging topics for students by deconstructing intricate genetic con-
cepts, sequences, and processes step-by-step in a visual format.
All Images from the Text
More than 500 illustrations can be downloaded as JPEGs and PowerPoint slides. Use
high-resolution images with enlarged labels to project clearly for lecture hall presen-
tations. Additionally, these JPEG and PowerPoint files are available without labels
for easy customization in PowerPoint.
67 Continuous-Play Animations
A comprehensive set of animations, updated and expanded for the eleventh edition,
covers everything from basic molecular genetic events and lab techniques to analyzing
crosses and genetic pathways. The complete list of animations appears on page xix.
xviii Preface
Assessment Bank
This resource brings together a wide selection of genetics problems for use in test-
ing, homework assignments, or in-class activities. Searchable by topic and pro-
vided in MS Word format, as well as in LaunchPad and Diploma, the assessment
bank offers a high level of flexibility.
Animations
Sixty-seven animations are fully integrated with the content and figures in the text
chapters. These animations are available on the LaunchPad and the Book Compan-
ion site.
CHAPTER 1
A Basic Plant Cross (Figure 1-3)
The Central Dogma (Figure 1-10)
CHAPTER 2
Mitosis (Chapter Appendix 2-1)
Meiosis (Chapter Appendix 2-2)
X-Linked Inheritance in Flies (Figure 2-17)
CHAPTER 3
Punnett Square and Branch Diagram Methods for Predicting the Outcomes
of Crosses (Figure 3-4)
Meiotic Recombination Between Unlinked Genes by Independent Assortment
(Figures 3-8 and 3-13)
Analyzing a Cross: A Solved Problem (Solved Problem 2)
CHAPTER 4
Crossing Over Produces New Allelic Combinations (Figures 4-2 and 4-3)
Meiotic Recombination Between Linked Genes by Crossing Over (Figure 4-7)
A Molecular Model of Crossing Over (Figure 4-21)
A Mechanism of Crossing Over: A Heteroduplex Model (Figure 4-21)
A Mechanism of Crossing Over: Genetic Consequences of the Heteroduplex Model
Mapping a Three-Point Cross: A Solved Problem (Solved Problem 2)
CHAPTER 5
Bacterial Conjugation and Mapping by Recombination (Figures 5-11 and 5-17)
CHAPTER 6
Interactions Between Alleles at the Molecular Level, RR: Wild-Type
Interactions Between Alleles at the Molecular Level, rr: Homozygous
Recessive, Null Mutation
Interactions Between Alleles at the Molecular Level, r ′r ′: Homozygous
Recessive, Leaky Mutation
Interactions Between Alleles at the Molecular Level, Rr: Heterozygous,
Complete Dominance
Screening and Selecting for Mutations
A Model for Synthetic Lethality (Figure 6-20)
CHAPTER 7
DNA Replication: The Nucleotide Polymerization Process (Figure 7-15)
DNA Replication: Coordination of Leading and Lagging Strand Synthesis
(Figure 7-20)
DNA Replication: Replication of a Chromosome (Figure 7-23)
xx Preface
CHAPTER 8
Transcription in Prokaryotes (Figures 8-7 to 8-10)
Transcription in Eukaryotes (Figures 8-12 and 8-13)
Mechanism of RNA Splicing (Figures 8-16 and 8-17)
CHAPTER 9
Peptide-Bond Formation (Figure 9-2)
tRNA Charging (Figure 9-7)
Translation (Figure 9-14 to 9-16)
Nonsense Suppression at the Molecular Level: The rod ns Nonsense Mutation
(Figure 9-18)
Nonsense Suppression at the Molecular Level: The tRNA Nonsense Suppressor
(Figure 9-18)
Nonsense Suppression at the Molecular Level: Nonsense Suppression of the rod ns
Allele (Figure 9-18)
CHAPTER 10
Polymerase Chain Reaction (Figure 10-3)
Plasmid Cloning (Figure 10-9)
Finding Specific Cloned Genes by Functional Complementation: Functional
Complementation of the Gal− Yeast Strain and Recovery of the Wild-Type
GAL gene
Finding Specific Cloned Genes by Functional Complementation: Making a Library
of Wild-Type Yeast DNA
Finding Specific Cloned Genes by Functional Complementation: Using the Cloned
GAL Gene as a Probe for GAL mRNA
SDS Gel Electrophoresis and Immunoblotting
Dideoxy Sequencing of DNA (Figure 10-17)
Creating a Transgenic Mouse (Figures 10-29 and 10-30)
CHAPTER 11
Regulation of the Lactose System in E. coli: Assaying Lactose Presence/Absence
Through the Lac Repressor (Figure 11-6)
Regulation of the Lactose System in E. coli: OC lac Operator Mutations
(Figure 11-8)
Regulation of the Lactose System in E. coli: I− Lac Repressor Mutations
(Figure 11-9)
Regulation of the Lactose System in E. coli: IS Lac Superrepressor Mutations
(Figure 11-10)
CHAPTER 12
Three-Dimensional Structure of Nuclear Chromosomes (Figure 12-11)
Gal4 Binding and Activation (Figures 12-6 through 12-9)
Chromatin Remodeling (Figures 12-13 and 12-14)
CHAPTER 13
Drosophila Embryonic Development
Sex Determination in Flies (Figure 13-23)
CHAPTER 14
DNA Microarrays: Using an Oligonucleotide Array to Analyze Patterns of
Gene Expression (Figure 14-20)
DNA Microarrays: Synthesizing an Oligonucleotide Array
Yeast Two-Hybrid Systems (Figure 14-21)
Preface xxi
CHAPTER 15
Replicative Transposition (Figure 15-9)
Life Cycle of a Retrovirus (Figure 15-11)
The Ty1 Mechanism of Retrotransposition (Figures 15-13 and 15-14)
CHAPTER 16
Replication Slippage Creates Insertion or Deletion Mutations (Figure 16-8)
UV-Induced Photodimers and Excision Repair (Figure 16-19)
Base-Excision Repair, Nucleotide Excision Repair, and Mismatch Repair
(Figures 16-20, 16-22, and 16-23)
CHAPTER 17
Autotetraploid Meiosis (Figure 17-6)
Meiotic Nondisjunction at Meiosis I (Figure 17-12)
Meiotic Nondisjunction at Meiosis II (Figure 17-12)
Chromosome Rearrangements: Paracentric Inversion, Formation of
Paracentric Inversions (Figure 17-27)
Chromosome Rearrangements: Paracentric Inversion, Meiotic Behavior
of Paracentric Inversions (Figure 17-28)
Chromosome Rearrangements: Reciprocal Translocation, Formation of
Reciprocal Translocations (Figure 17-30)
Chromosome Rearrangements: Reciprocal Translocation, Meiotic Behavior
of Reciprocal Translocations (Figure 17-30)
Chromosome Rearrangements: Reciprocal Translocation, Pseudolinkage
of Genes by Reciprocal Translocations (Figure 17-32)
Acknowledgments
We extend our thanks and gratitude to our colleagues who reviewed this edition and whose insights and advice were
most helpful:
Shirlean Goodwin, University of Memphis Ann Murkowski, North Seattle Community College
Topher Gee, UNC Charlotte Saraswathy Nair, University of Texas at Brownsville
John Graham, Berry College Sang-Chul Nam, Texas A&M International University
Theresa Grana, University of Mary Washington Scot Nelson, University of Hawaii at Manoa
Janet Guedon, Duquesne University Brian Nichols, University of Illinois at Chicago
Patrick Gulick, Concordia University Todd Nickle, Mount Royal University
Richard Heineman, Kutztown University Juliet Noor, Duke University
Anna Hicks, Memorial University Mohamed Noor, Duke University
Susan Hoffman, Miami University Daniel Odom, California State University, Northridge
Stanton Hoegerman, College of William and Mary Kirk Olsen, East Los Angeles College
Margaret Hollingsworth, University at Buffalo Kavita Oommen, Georgia State University
Nancy Huang, Colorado College Maria Orive, University of Kansas
Jeffrey Hughes, Millikin University Laurie Pacarynuk, University of Lethbridge
Varuni Jamburuthugoda, Fordham University Patricia Phelps, Austin Community College
Pablo Jenik, Franklin & Marshall College Martin Poenie, University of Texas at Austin
Aaron Johnson, University of Colorado School Jennifer Powell, Gettysburg College
of Medicine Robyn Puffenbarger, Bridgewater College
Anil Kapoor, University of La Verne Jason Rauceo, John Jay College (CUNY)
Jim Karagiannis, University of Western Ontario Eugenia Ribiero-Hurley, Fordham University
Kathleen Karrer, Marquette University Ronda Rolfes, Georgetown University
Jessica Kaufman, Endicott College Edmund Rucker, University of Kentucky
Darrell Killian, Colorado College Jeffrey Sands, Lehigh University
Dennis Kraichely, Cabrini College Monica Sauer, University of Toronto at Scarborough, UTSC
Anuj Kumar, University of Michigan Ken Saville, Albion College
Janice Lai, Austin Community College Pratibha Saxena, University of Texas at Austin
Evan Lau, West Liberty University Jon Schnorr, Pacific University
Min-Ken Liao, Furman University Malcolm Schug, University of North Carolina at
Sarah Lijegren, University of Mississippi Greensboro
Renyi Liu, University of California, Riverside Deborah Schulman, Lake Erie College
Diego Loayza, Hunter College Allan Showalter, Ohio University
James Lodolce, Loyola University Chicago Elaine Sia, University of Rochester
Joshua Loomis, Nova Southeastern University Robert Smith, Nova Southeastern University
Amy Lyndaker, Ithaca College Joyce Stamm, University of Evansville
Jessica Malisch, Claremont McKenna College Tara Stoulig, Southeastern Louisiana University
Patrick Martin, North Carolina A&T State University Julie Torruellas Garcia, Nova Southeastern University
Presley Martin, Hamline University Virginia Vandergon, California State University,
Dmitri Maslov, University of California, Riverside Northridge
Maria Julia Massimelli, Claremont McKenna College Charles Vigue, University of New Haven
Endre Mathe, Vasile Goldis Western University of Arad Susan Walsh, Rollins College
Herman Mays, University of Cincinnati Michael Watters, Valparaiso University
Thomas McGuire, Penn State Abington Roger Wartell, Georgia Institute of Technology
Mark Meade, Jacksonville State University Matthew White, Ohio University
Ulrich Melcher, Oklahoma State University Dwayne Wise, Mississippi State University
Philip Meneely, Haverford College Andrew Wood, Southern Illinois University
Ron Michaelis, Rutgers University Mary Alice Yund, UC Berkeley Extension
Chris Mignone, Berry College Malcom Zellars, Georgia State University
Sarah Mordan-McCombs, Franklin College of Indiana Deborah Zies, University of Mary Washington
Preface xxiii
Mr. Jenner. Would you stand, please, and take the oath?
Do you solemnly swear in your testimony before this Commission
that you will tell the truth, the whole truth, and nothing but the
truth, so help you God?
Mr. Biggio. I will.
Mr. Jenner. Would you state your full name, and spell it, please?
Mr. Biggio. William S. Biggio, [spelling] B-i-g-g-i-o.
Mr. Jenner. And you are a member of the Dallas City Police Force?
Mr. Biggio. That’s right.
Mr. Jenner. Are you in any particular division, do you have a
particular assignment?
Mr. Biggio. I am with the special service bureau, criminal
intelligence section.
Mr. Jenner. Now, I am Albert E. Jenner, Jr., one of the members
of the legal staff of the Warren Commission, with which you are
familiar, and this item has come to my attention recently through Mr.
Davis of the attorney general’s office of the Texas staff and while I
appreciate the fact that at the moment it is third hand or hearsay, as
we lawyers call it, I would just like to have your report on it—which
we will seek to run down—as I understand Mr. Davis and the FBI are
undertaking the investigation; is that right?
Mr. Davis. Yes, sir.
Mr. Biggio. I have since talked to them also.
Mr. Davis. Since we talked?
Mr. Biggio. Yes, sir.
Mr. Jenner. You appreciate the existence of the President’s
Commission and what the President’s Commission is engaged in, in
the investigating of the assassination of President Kennedy and
many members of your force have been very helpful to us and have
been appearing these last 2 weeks by considerable number. Tell us
about this whole incident from the beginning—when it first came to
your attention, who brought it to your attention and what developed
thereafter?
Mr. Biggio. There was a friend of mine—she is a woman who I
know through my wife. She formerly was employed at the same
location that my wife is, and she called me at work following Ruby’s
killing of Oswald. She said that a friend of hers had been into a
restaurant in the downtown area and a mechanic had come in and
had made mention of the fact that Oswald drove Ruby’s car for
approximately a 2-week period that he knew of, that Oswald had
brought the car there for repairs to his garage.
The friend did not know where the garage was, did not know the
mechanic’s name. The woman who called me didn’t want to give her
friend’s name and get his name involved if she could possibly help it.
Mr. Jenner. Who was it that called you?
Mr. Biggio. Is it necessary for me to give that name? I believe
with the information that was given me, it will not be necessary.
Mr. Jenner. Has the information been furnished the FBI?
Mr. Biggio. No; it has not. I believe with the information we get
to further on it will show that her name isn’t needed.
Mr. Jenner. All right.
Mr. Biggio. I don’t object to giving her name except that she
asked me not to give it.
Mr. Jenner. All right; she didn’t want any publicity, is that it?
Mr. Biggio. No; she doesn’t want any publicity on it. I don’t know
why people are so scared of things like this, but if they get into court
or before a panel or anything like that—at any rate, her friend
doesn’t want his name used either, but I talked to my lieutenant
about it, Lieutenant Revill, and he suggested that we go ahead and
write it up on the grounds that by searching through the material in
Ruby’s apartment and also through the material that had been taken
from his automobile, we could possibly find a garage where a
mechanic had done some work on his car. We would be able to
contact the mechanic in that way without involving the two people
who had called the information in.
When we did get photostatic copies of the material that had
been taken out of Ruby’s car and his apartment, we found no
evidence of any garage work that had been done or any actual
mechanical work that had been done on his car recently. So, I called
my friend back and asked her again if she could contact the man
who had given her the information and see if he would be willing to
talk to us about it. She called him back and then she called me and
she said she had made an error in saying it was in the downtown
area, that the place was out on Lovers Lane, directly across from—I
have the address in here——
Mr. Jenner. Is it 5060 W. Lovers Lane?
Mr. Biggio. Well; she didn’t have the address itself—it was
directly across from the Jungle Hut which is in the 5000 block of
Lovers Lane.
Mr. Jenner. Lovers Lane is a street name?
Mr. Biggio. Yes; Lovers Lane is a street. We sent an officer out
there, Detective Hellinghousen, F. A.
Mr. Jenner. Francis A. Hellinghousen [spelling] H-e-l-l-i-n-g-h-o-u-
s-e-n?
Mr. Biggio. That is correct; yes, sir.
Mr. Jenner. Of the Dallas City Police?
Mr. Biggio. Yes, sir. He went to that particular area—there are
two cafes across the street there in the 5000 block from the
particular location that the lady friend of mine said. One of them was
the Cafe Coffee Shop, was the name of it—the Cafe Coffee Shop. It
was closed up at that time. Now, this took place approximately 3
weeks after the shooting. It was closed—ordinarily through our
bureau we can find out who the owner was of such a place, because
we keep the records of everyone through the beer licenses which we
have to keep in our particular bureau, but this particular place did
not have a beer license. It did not deal in beer.
It had been closed—we couldn’t find out who the owner was, so
I sent Officer Hellinghousen and requested him to go by and talk to
the woman who had originally given me that information and see if
she would be willing to give him the same thing—the man’s name.
Officer Hellinghousen went by and talked to her and she gave him
the man’s name and at that particular time the man was attending a
real estate convention which was here and being held here in Dallas
and the word was sent to him from the company that he works for,
the Bill Hardy Real Estate Co.—word was sent to the man, his name
was Chesher [spelling] C-h-e-s-h-e-r—Bill was his first name. I
believe it is correct—William R. He lives on Lupton Street.
Mr. Jenner. Is he still alive?
Mr. Biggio. No, sir. I tried to contact Hellinghousen today. Mr.
Davis had gone up to talk to Captain Gannaway in regard to that
report. I had understood that Hellinghousen had written a report
from what he had learned from Mr. Chesher and I tried to contact
him and could not, after Captain Gannaway had called me, so I went
out to the Bill Hardy Real Estate Co. where Chesher works, and I
talked to the manager of that company who is Wey, Jr. The location
of the real estate company is 6340 E. Mockingbird Lane. Mr. Wey
informed us that Bill Chesher died night before last of a heart attack
in the hospital here. We then asked him if he had talked to Chesher
any about hearing this mechanic talking in the cafe and he said, “No,
he had heard some talk of it, though and he knew one man who had
talked to him” and he called in another employee of the company,
Mr. John P. [spelling] S-c-h-n-i-t-z-i-u-s, who is also an employee of
the Bill Hardy Real Estate Co. and he told us that Chesher told him
the same thing, that the mechanic had came in and sat by him and
it was—that it took place at approximately 10 o’clock at night. He
was leaving town—he was going out of town. He stopped there to
get coffee and a sandwich and the man came in while he was there
and he had given no description of the mechanic other than that he
was short and was dressed in work clothes and that the clothes were
greasy and that’s the information that he had, and I believe the man
was telling the truth when he said he was a mechanic and that’s as
far as we have been able to go.
Mr. Jenner. What is it that the mechanic is alleged to have said?
Mr. Biggio. He said that Oswald had been driving Ruby’s car for
approximately 2 weeks and that he had brought the car into his
garage for repairs, but he did not mention the name of the garage
or the type of repairs, the type of automobile or anything else.
Now, we, of course—just as soon as that came through, there
were checks made on the repairs on Ruby’s automobile. His
automobile was parked regularly, just a short distance up from the
Carousel Club at the old Adolphus Hotel parking garage and also
mechanical work had been done at that location, and the only other
place we can find out where it had been to any type of garage at all
was from receipts in his car and they were apparently for gas and oil
and such things as that—no mechanical work whatsoever, so we
didn’t put much stock in the report, since it was third hand to start
off with.
Also, we made an error ourselves—Hellinghousen thought when
we brought that information back about Chesher that I would write
up the report and I thought he was preparing the report, since he
was the one who actually contacted the man and no report was
made, but I’m sure the report went to the FBI, but there is no name
in the original report connecting anybody with it and there was
nothing in that that we could check on except the way we thought
was through the mechanical repair bills and they would possibly be
in the car.
Mr. Jenner. You have told me all the incidents from the beginning
to the present time?
Mr. Biggio. Yes, sir.
Mr. Jenner. And what you and your fellow officers have done with
respect to running this down?
Mr. Biggio. Yes, sir. I might add that the gentlemen out at Bill
Hardy’s Real Estate Co. were very cooperative and they said they
would be willing to talk to any one of you. This lady who called me
was very worried about being called herself or about Mr. Chesher
possibly being called and him not liking it.
Mr. Jenner. Now, the lady who reported it to you, she was not
present—it had been a report to her?
Mr. Biggio. She was not present. That’s the reason I say it was
third-hand information. It was written up in the report that way,
although I considered her reliable. The information was third-hand
and there is no way of actually telling. We have to evaluate all the
information that comes through and that generally is the reason we
make followup investigation prior to turning in a report. In this
particular case we were to turn in our information right on through
and let the FBI do it; but as you can see, the FBI would have
nothing to go on.
Mr. Jenner. Well, they have got what you reported and we’ll see
what they turn up.