28.1 Introduction 28.2 Transforming viruses carry oncogenes 28.3 Early genes of DNA transforming viruses have multifunction oncogenes 28.4 Retroviruses activate or incorporate cellular genes 28.5 Retroviral oncogenes have cellular counterparts 28.6 Ras oncogenes can be detected in a transfection assay 28.7 Ras proto-oncogenes can be activated by mutation at specific positions 28.8 Nondefective retroviruses activate proto-oncogenes 28.9 Proto-oncogenes can be activated by translocation 28.10 The Philadelphia translocation generates a new oncogene 28.11 Oncogenes code for components of signal transduction cascades 28.12 Growth factor receptor kinases can be mutated to oncogenes 28.13 Src is the prototype for the proto-oncogenic cytoplasmic tyrosine kinases 28.14 Oncoproteins may regulate gene expression 28.15 RB is a tumor suppressor that controls the cell cycle 28.16 Tumor suppressor p53 suppresses growth or triggers apoptosis

Gene clusters are formed by duplication and divergence Sequence divergence is the basis for the evolutionary clock Pseudogenes are dead ends of evolution Unequal crossing-over rearranges gene clusters Genes for rRNA form tandem repeats ( The repeated genes for rRNA maintain constant sequence) Crossover fixation could maintain identical repeats Satellite DNAs often lie in heterochromatin Arthropod satellites have very short identical repeats Mammalian satellites consist of hierarchical repeats Minisatellites are useful for genetic mapping

5.1 Introduction 5.2 Transfer RNA is the adapter 5.3 Messenger RNA is translated by ribosomes 5.4 The life cycle of bacterial messenger RNA 5.5 Translation of eukaryotic mRNA 5.6 The 5 end of eukaryotic mRNA is capped 5.7 The 3 terminus is polyadenylated 5.8 Bacterial mRNA degradation involves multiple enzymes

母性影响表现的遗传现象与细胞质遗传十 分相似，但是这种遗传不是由细胞质基因组所 决定的，而是由核基因的产物积累在卵细胞中 的物质所决定的。 例如：锥实螺的外壳旋转方向的遗传就是母性 影响一个比较典型的例证

根据待选基因相关信息→确定筛选方法和条件 从基因库中筛选、分离基因。 多数方法是利用一段核苷酸序列DNA、cDNA或 寡聚核苷酸)或抗体作探针(Pobe),用放射性同位素或 非放射性同位素标记探针→筛选基因库

8.1 Introduction 8.2 Chaperones may be required for protein folding 8.3 Post-translational membrane insertion depends on leader sequences 8.4 A hierarchy of sequences determines location within organelles 8.5 Signal sequences initiate translocation 8.6 How do proteins enter and leave membranes? 8.7 Anchor signals are needed for membrane residence 8.8 Bacteria use both co-translational and post-translational translocation 8.9 Pores are used for nuclear ingress and egress 8.10 Protein degradation by proteasomes

7.1 Introduction 7.2 Codon-anticodon recognition involves wobbling 7.3 tRNA contains modified bases that influence its pairing properties 7.4 (There are sporadic alterations of the universal code) 7.5 tRNAs are charged with amino acids by synthetases 7.6 Accuracy depends on proofreading 7.7 Suppressor tRNAs have mutated anticodons that read new codons 7.8 The accuracy of translation 7.9 tRNA may influence the reading frame

DNA是遗传物质 DNA为双螺旋 DNA的复制是半保留的 通过碱基配对进行核酸杂交 突变改变了DNA的序列 突变集中于热点 顺反子是单个DNA片断 多重等位基因的种类

26.1 Introduction 26.2 Carriers and channels form water soluble paths through the membrane 26.3 Ion channels are selective 26.4 Neurotransmitters control channel activity 26.5 G proteins may activate or inhibit target proteins 26.6 G proteins function by dissociation of the trimer 26.7 Growth factor receptors are protein kinases 26.8 Receptors are activated by dimerization 26.9 Receptor kinases activate signal transduction pathways

17.1 Introduction 17.2 The mating pathway is triggered by pheromone-receptor interactions 17.3 The mating response activates a G protein 17.4 Yeast can switch silent and active loci for mating type 17.5 The MAT locus codes for regulator proteins 17.6 Silent cassettes at HML and HMR are repressed 17.7 Unidirectional transposition is initiated by the recipient MAT locus 17.8 Regulation of HO expression 17.9 Trypanosomes switch the VSG frequently during infection 17.10 New VSG sequences are generated by gene switching 17.11 VSG genes have an unusual structure 17.12 The bacterial Ti plasmid causes crown gall disease in plants 17.13 T-DNA carries genes required for infection 17.14 Transfer of T-DNA resembles bacterial conjugation 17.15 Selection of amplified genomic sequences 17.16 Transfection introduces exogenous DNA into cells 17.17 Genes can be injected into animal eggs 17.18 ES cells can be incorporated into embryonic mice 17.19 Gene targeting allows genes to be replaced or knocked out