From in situ hybridizations, five different YACs containing genomic fragments were known to hybridize to one specific chromosome band of the human genome. Genomic DNA was digested with a long-cutter restriction enzyme, and radioactively labeled YACs were each hybridized to blots of the digest. The autoradiogram was as follows:

Three genes, leu2, ade3, and mata, were cloned in yeast. A Neurospora geneticist wanted to find out if Neurospora had these three genes and, if so, wanted to clone the Neurospora equivalents. As a first step to this analysis, he hybridized the clones as radioactive probes to PFGE preparations of Neurospora chromosomes, with the following results. Which genes are present in Neurospora, and what chromosomes are they on?

A Neurospora geneticist wanted to clone the gene cys-1, which was believed to be near the centromere on chromosome 5. Two RFLP markers (RFLP1 and RFLP2) were available in that vicinity, so he made the cross

In a certain haploid fungus, there had been extensive genetic analysis, including genetic mapping, and four linkage groups had been developed, suggesting four chromosomes. However, the chromosomes were very small and difficult to see under the microscope, so it was not known if there really were four chromosomes. The advent of PFGE technology showed that there are four chromosomes. However, the linkage groups still needed to be assigned to these chromosomes. To begin this process, a cloned gene P was used in a Southern analysis with a PFGE preparation from wild type and from two translocations that were known from genetic studies to involve linkage groups 1 and 4 in one case and 2 and 4 in the other. The results follow:

A cloned gene from Arabidopsis is used as a radioactive probe against DNA samples from cabbage (in the same plant family) digested by three different restriction enzymes. For enzyme 1, there were three radioactive bands on the autoradiogram; for enzyme 2, there was one band; and, for enzyme 3, there were two bands. How can these results be explained?

Five YAC clones of human DNA (YAC-A through YAC-E) were tested for sequence-tagged sites STS1 through STS7. The results are shown in the following table, in which a plus sign shows that the YAC contains that STS.

Seven humanrodent radiation hybrids were obtained and tested for six different human genome molecular markers A through F. The results are shown here, where a plus sign indicates the presence of a marker.** RADIATION HYBRIDS***

A RAPD primer amplified two bands in Aspergillus nidulans haploid strain 1 and no bands in Aspergillus nidulans strain 2 (which was from a different country). These strains were crossed, and seven progeny were analyzed. The results were as follows:

A Caenorhabditis contig for one region of chromosome 2 is as follows, where A through H are cosmids:

A geneticist succeeds in maintaining three colonies of humanmouse hybrid cells. The only human chromosomes retained by the hybrid cells are those indicated by pluses:

The geneticist tests each of the colonies for the presence of five enzymes (a, b, g, d, and e) with the following results: a is active only in colony C, b is active in all three colonies, g is active only in colonies B and C, d is active only in colony B, and e shows no activity in any colony. What can the geneticist conclude about the locations of the genes responsible for these enzyme activities?

Consider the following set of eight hybridized humanmouse cell lines:

Each cell line may carry an intact (numbered) chromosome (+), only its long arm (q), or only its short arm (p), or it may lack the chromosome ().

The following human enzymes were tested for their presence (+) or absence () in cell lines AH:

Identify the chromosome carrying each enzyme locus. Where possible, identify the chromosome arm.

(Problem 11 is from L. A. Snyder, D. Freifelder, and D. L. Hartl, General Genetics. Jones and Bartlett, 1985.)

A certain disease is inherited as an autosomal dominant N. It was noted that some patients carry reciprocal translocations in which one of the chromosomes involved is always chromosome 3 and the break is always in band 3q3.1. Four molecular probes (a through d) are known to hybridize in situ to this band, but their order is not known. In the translocations, only probe c hybridizes to chromosome 3 carrying a part of another chromosome, and probes a, b, and d always hybridize to the translocated fragment of chromosome 3.
a. Draw diagrams that illustrate the meaning of these findings.

b. How would you use this information for positional cloning of the normal allele n?

c. Once n is cloned, how would you use this clone to investigate the nature of the mutations in disease patients who do not have translocations?

The gene for the autosomal dominant disease shown in this pedigree is thought to be on chromosome 4, so five RFLPs (15) mapped on chromosome 4 were tested in all family members. The results are also shown in the diagram; the superscripts represent different alleles of the RFLP loci.

Let's say that you undertake a study of hybridized human and mouse cells because you want to map part of human chromosome 17. Three loci on this chromosome, a, b, and c, are concerned with making the compounds a, b, and call of which are essential for growth and are present in mice as well as humans. You fuse mouse cells that are phenotypically a b c with a⁺ b⁺ c⁺ human cells. Assume that you find a hybrid in which the only human component is the right arm of chromosome 17 (17R), translocated by some unknown mechanism to a mouse chromosome. The hybrid can make the compounds a, b, and c. Then you treat cells with adenovirus, which causes chromosome breaks. Assume that you can isolate 200 lines in which bits of the translocated 17R have been clipped off. You test these lines for the ability to make a, b, and c, and obtain the following results:

A couple has three children with cystic fibrosis (CF). Their oldest son has recently married his second cousin. He has molecular testing done to determine if there is a chance that he may have children with CF. Three probes detecting RFLPs known to be very closely linked to the CF gene were used to assess the genotypes in this family. Answer the following questions, describing your logic.
a. Is this man homozygous normal or a carrier?

b. Are his three normal siblings homozygous normal or carriers?

c. From which parent did each carrier inherit the disease allele?