基于高通量测序的厚唇裸重唇鱼微卫星分子标记筛选

本研究对厚唇裸重唇鱼(Gymnodiptychus pachycheilus)基因组进行Illumina HiSeq高通量测序，共获得85 905条序列，包含567 200个微卫星位点，从中筛选出15个微卫星位点，采用雅砻江新龙种群和黄河渭河种群对其多态性进行了验证。新龙种群中，15个位点的平均等位基因数为6.9(3 ~ 13)，观测杂合度(Ho)为0.712 4，多态信息含量(PIC)为0.630 3，有8个位点显著偏离哈迪-温伯格平衡，1对位点表现出连锁。渭河种群中，15个位点的平均等位基因数为8.4(4 ~ 16)，观测杂合度(Ho)为0.719 5，多态信息含量(PIC)为0.680 7，有7个位点显著偏离了哈迪-温伯格平衡，4对位点表现出连锁。筛选获得的15个微卫星位点多态性较高，适合用于厚唇裸重唇鱼种群遗传学研究。     

Genetic evidence that both dNTP-stabilized and strand slippage mechanisms may dictate DNA polymerase errors within mononucleotide microsatellites

Mononucleotide microsatellites are tandem repeats of a single base pair, abundant within coding exons and frequent sites of mutation in the human genome. Because the repeated unit is one base pair, multiple mechanisms of insertion/deletion (indel) mutagenesis are possible, including strand-slippage, dNTP-stabilized, and misincorportion-misalignment. Here, we examine the effects of polymerase identity (mammalian Pols α, β, κ, and η), template sequence, dNTP pool size, and reaction temperature on indel errors during in vitro synthesis of mononucleotide microsatellites. We utilized the ratio of insertion to deletion errors as a genetic indicator of mechanism. Strikingly, we observed a statistically significant bias toward deletion errors within mononucleotide repeats for the majority of the 28 DNA template and polymerase combinations examined, with notable exceptions based on sequence and polymerase identity. Using mutator forms of Pol β did not substantially alter the error specificity, suggesting that mispairing-misalignment mechanism is not a primary mechanism. Based on our results for mammalian DNA polymerases representing three structurally distinct families, we suggest that dNTP-stabilized mutagenesis may be an alternative mechanism for mononucleotide microsatellite indel mutation. The change from a predominantly dNTP-stabilized mechanism to a strand-slippage mechanism with increasing microsatellite length may account for the differential rates of tandem repeat mutation that are observed genome-wide.     

Trinucleotide Repeats as Bait for Vectorette PCR: A Tool for Developing Genetic Mapping Markers

Trinucleotide repeats are common within gene coding regions and could serve as beacons to locate genes. Five of the most common trinucleotide repeats in an Actinidia (kiwifruit) expressed sequence tag (EST) database were found to be (ACC)₄, (CAC)₄, (CCA)₄, (CTC)₄, and (TGG)₄. These repeats, with or without an artificial 5′-end tail, were tested by vectorette PCR against genomic DNA from Actinidia chinensis. Eighty-nine randomly selected clones showed an average insert size of 383 bp, with a maximum of 1,151 bp and a minimum of 78 bp. Two-thirds of the clones contained the artificial tail attached to the trinucleotide, showing a slight advantage of possessing such a tail during annealing and amplification. The sequences were searched against the Actinidia EST database and GenBank. Of the 89 clones, 33 had a significant hit (expect value < e⁻¹⁵). Twenty-four of those clones matched an Actinidia EST. Twenty-one clones contained one or more simple sequence repeats. This methodology can be applied by conventional cloning and sequencing methods or by high throughput pyrosequencing technologies to develop genetic markers and also for gene mining in species with little or no genetic/genomic resources.     

Evaluation of cadmium genotoxicity in Lactuca sativa L. using nuclear microsatellites

Cadmium (Cd) is a non-essential element and is a widespread environmental pollutant. Exposure to cadmium can result in cytotoxic, carcinogenic and mutagenic effects. Mutagenesis is indicative of genetic instability and can be assayed using microsatellites. Microsatellites or simple sequence repeats (SSRs) are composed of tandem repeats of short sequence motifs (1–6 bp) that are polymorphic, mainly in the number of tandem repeated units. Therefore, chromosomic mutations like inversion, deletion or translocation and point mutations can be detected by this type of molecular marker. In this study we have evaluated the mutagenic/genotoxic effects of cadmium in lettuce (Lactuca sativa L.). Five-week-old lettuce plants grown in a modified Hoagland's medium were exposed for a further 14 days to a medium containing 100 μM Cd(NO₃)₂. Genomic DNA was extracted from lettuce leaves and roots, harvested at days 0, 1, 3, 7 and 14, and nine SSRs were tested, amplified and analysed to evaluate microsatellite instability (MSI). Mutagenic effects of cadmium on microsatellite DNA loci were assessed and no MSI was observed in the used markers.     

Isolation and characterization of thirteen microsatellite loci in four diploid species of Ranunculus cantonensis polyploid complex

Ranunculus is a cosmopolitan genus, and the evolution of the genus has been influenced by both polyploidy and hybridization. The interactions between some species of Ranunculus are regarded as a natural model system for studying hybridization. Four diploid species of the R. cantoniensis polyploid complex have relatively little reproductive isolation from each other, and they form a complicated hybrid pool in a multispecies hybrid zone. To clarify the genetic structure and spatiotemporal dynamics of gene flow in this multispecies hybrid zone, 13 polymorphic microsatellite loci were isolated from R. silerifolius var. dolicanthus. The loci's characteristics were observed in 30 individuals. The number of alleles per locus ranged from 6 to 20, and the PIC values ranged from 0.350 to 0.914. Eleven loci were significantly biased from the Hardy–Weinberg equilibrium. The 13 microsatellite loci were shown to be successfully amplified in three other related species. These polymorphic microsatellites will be powerful molecular tools for further studies of the Ranunculus genetic structure and gene flow.     

Wild gibbons' parentage tested by non-invasive DNA sampling and PCR-amplified polymorphic microsatellites

Elucidating the genetic relationships among members of a social group is indispensable in studying any social system of primates.Hylobates spp. are believed to be monogamous, although some long-term monitoring studies have provided conflicting evidence. We applied a parentage testing technique to a group ofHylobates muelleri in the wild. Forty-five microsatellite loci were screened in the 12 unrelated gibbons' DNA, and 16 of the 45 loci were found to be polymorphic. Hair and fecal samples from 15 gibbons in the field were collected non-invasively. In each sample, the 16 polymorphic loci were amplified by PCR using appropriate primer pairs and separated by electrophoresis. We estimated three pairs of parents-offspring, a pair each of both father-offspring, and mother-offspring genetic relationships. Further, in two of the five cases, we revealed the family a subadult lived with was not a natal one of the subadult. The non-invasive sampling methods and polymorphic primer pairs used in this study would greatly enhance the understanding of gibbon's society in the wild.     

Application of two microsatellite sequences in wheat storage proteins as molecular markers

In eukaryotes, tandem arrays of simple-sequence repeat sequences can find applications as highly variable and multi-allelic PCR-based genetic markers. In hexaploid bread wheat, a large-genome inbreeding species with low levels of RFLP, di- and trinucleotide tandem repeats were found in 22 published gene sequences, two of which were converted to PCR-based markers. These were shown to be genome-specific and displayed high levels of variation. These characteristics make them especially suitable for intervarietal breeding applications.