Microalgal assemblages response to water quality remediation in coastal waters of Perth, Australia.

Nutrient reduction is an essential environmental policy for water quality remediation, but climate change can offset the ecological benefits of nutrient reduction and lead to the difficulty of environmental evaluation. Here, based on the records of three lipid microalgal biomarkers and stable isotopes of carbon and nitrogen in two sediment cores from the embayment of Perth, Australia, we reconstructed the microalgal biomasses (diatoms, dinoflagellates and coccolithophores) over the past century and evaluated the ecological effects of nutrient reduction on them, using Change Point Modeling (CPM) and redundancy analysis (RDA). The CPM result showed that total microalgal biomarkers increased by 25% and 51% in deep and shallow areas, respectively, due to nutrient enrichment caused by industrial wastewater in the 1950s and the causeway construction in the 1970s, and dinoflagellates were beneficiaries of eutrophication. The nutrient reduction policy since the 1980s had not decreased total microalgal biomass, and diatoms were beneficiaries of this period. RDA based on time series of sediment cores and water monitoring data revealed that the increase of sea-surface temperature and the decrease of rainfall since the 1980s may be important factors sustaining the high total microalgal biomass and increasing the degree of diatom dominance. The result also indicated that the variations of microalgal assemblages may better explain the effect of nutrient reduction rather than total microalgal biomass.

Sources and radiocarbon ages of aerosol organic carbon along the east coast of China and implications for atmospheric fossil carbon contributions to China marginal seas.

Aerosol deposition is an important mechanism for the delivery of terrestrial organic carbon (OC) to marginal seas, but OC age characteristics of aerosols are not well constrained and their contributions to sediment OC burial have not been quantified. Total suspended particle samples were collected along the east coast of China at Changdao (CD), Qingdao (QD) and Huaniao Island (HNI), and were analyzed for total organic carbon (TOC) isotopes (13C and 14C) in order to bridge this information gap. TOC δ13C and Δ14C values ranged from -23.6 to -30.5‰, and -153 to -687‰, respectively, with the latter corresponding to 14C ages ranging from 1280 to 9260yr. Estimated contributions of fossil carbon to TOC based on 14C mass balance approach ranged from 26 to 73%, with strong seasonal variations in fossil carbon observed at CD. Fossil carbon at CD showed the highest proportion (73%) in winter, reflecting anthropogenic emissions and the lowest proportion (26%) in summer, caused by biomass contribution (annual ave., 52%±17%). In contrast, the fossil carbon at both QD (57-64%) and HNI (57-67%) dominated throughout the year, reflecting local anthropogenic influences and long-range transport. Mass balance estimates indicate that atmospheric deposition and riverine export accounted for 31% and 69% of fossil carbon inputs to the China marginal seas (CMS) respectively, with fossil carbon burial efficiencies approaching 100% in the CMS. On a global scale, an atmospheric fossil carbon deposition flux of 17.2TgCyr-1 was estimated, equivalent to 40% of the estimated fluvial flux to the ocean, and potentially accounting for 24-41% of fossil OC burial in marine sediments. Therefore, the atmospheric deposition constitutes an important source of fossil carbon to marine sediments, and could play a key role in regional and global scale OC budgets and biogeochemical cycles.

Paleoecological evidence for decadal increase in phytoplankton biomass off northwestern Australia in response to climate change.

Ocean warming can modify the phytoplankton biomass on decadal scales. Significant increases in sea surface temperature (SST) and rainfall in the northwest of Australia over recent decades are attributed to climate change. Here, we used four biomarker proxies (TEX86 index, long-chain n-alkanes, brassicasterol, and dinosterol) to reconstruct approximately 60-year variations of SST, terrestrial input, and diatom and dinoflagellate biomass in the coastal waters of the remote Kimberley region. The results showed that the most significant increases in SST and terrestrial input occurred since 1997, accompanied by an abrupt increase in diatom and dinoflagellate biomasses. Compared with the results before 1997, the average TEX86H temperature during 1997-2011 increased approximately 1°C, rainfall increased 248.2 mm, brassicasterol and dinosterol contents increased 8.5 and 1.7 times. Principal component analysis indicated that the warming SST played a more important role in the phytoplankton increase than increased rainfall and river discharge.

Evidences for increased expression variation of duplicate genes in budding yeast: from cis- to trans-regulation effects.

Duplicate genes tend to have a more variable expression program than singleton genes, which was thought to be an important way for the organism to respond and adapt to fluctuating environment. However, the underlying molecular mechanisms driving such expression variation remain largely unexplored. In this work, we first rigorously confirmed that duplicate genes indeed have higher gene expression variation than singleton genes in several aspects, i.e. responses to environmental perturbation, between-strain divergence, and expression noise. To investigate the underlying mechanism, we further analyzed a previously published expression dataset of yeast segregants produced from genetic crosses. We dissected the observed expression divergence between segregant strains into cis- and trans-variabilities, and demonstrated that trans-regulation effect can explain larger fraction of the expression variation than cis-regulation effect. This is true for both duplicate genes and singleton genes. In contrast, we found, between a pair of sister paralogs, cis-variability explains more of the expression divergence between the paralogs than trans-variability. We next investigated the presence of cis- and trans-features that are associated with elevated expression variations. For cis-acting regulation, duplicate genes have higher genetic diversity in their promoters and coding regions than singleton genes. For trans-acting regulation, duplicate and singleton genes are differentially regulated by chromatin regulators and transcription factors, and duplicate genes are more severely affected by the deletion of histone tails. These results showed that both cis-and trans-factors have great effect in causing the increased expression variation of duplicate genes, and explained the previously observed differences in transcription regulation between duplicate genes and singleton genes.

The cellular robustness by genetic redundancy in budding yeast.

The frequent dispensability of duplicated genes in budding yeast is heralded as a hallmark of genetic robustness contributed by genetic redundancy. However, theoretical predictions suggest such backup by redundancy is evolutionarily unstable, and the extent of genetic robustness contributed from redundancy remains controversial. It is anticipated that, to achieve mutual buffering, the duplicated paralogs must at least share some functional overlap. However, counter-intuitively, several recent studies reported little functional redundancy between these buffering duplicates. The large yeast genetic interactions released recently allowed us to address these issues on a genome-wide scale. We herein characterized the synthetic genetic interactions for ∼500 pairs of yeast duplicated genes originated from either whole-genome duplication (WGD) or small-scale duplication (SSD) events. We established that functional redundancy between duplicates is a pre-requisite and thus is highly predictive of their backup capacity. This observation was particularly pronounced with the use of a newly introduced metric in scoring functional overlap between paralogs on the basis of gene ontology annotations. Even though mutual buffering was observed to be prevalent among duplicated genes, we showed that the observed backup capacity is largely an evolutionarily transient state. The loss of backup capacity generally follows a neutral mode, with the buffering strength decreasing in proportion to divergence time, and the vast majority of the paralogs have already lost their backup capacity. These observations validated previous theoretic predictions about instability of genetic redundancy. However, departing from the general neutral mode, intriguingly, our analysis revealed the presence of natural selection in stabilizing functional overlap between SSD pairs. These selected pairs, both WGD and SSD, tend to have decelerated functional evolution, have higher propensities of co-clustering into the same protein complexes, and share common interacting partners. Our study revealed the general principles for the long-term retention of genetic redundancy.

Revisiting the contribution of cis-elements to expression divergence between duplicated genes: the role of chromatin structure.

Although divergence in expression is thought to be a hallmark of functional dispersal between paralogs postduplication, there is currently a limited understanding of the mechanisms underlying the necessary transcriptional alterations as recent studies have suggested that only a very small proportion of expression variation could be explained by transcriptional variation between paralogs. To further this understanding, we examined comprehensively curated regulatory interactions and genomewide nucleosome occupancy in budding yeast to specifically determine the contribution of cis-elements to expression divergence between extant duplicates. We found that divergence in activation by transcription factors plays a more important role in expression divergence of paralogs than previously appreciated; further, analysis of promoter chromatin structure demonstrated that differential nucleosome organization is coupled with divergent expression of paralogs. By incorporating information of cis-elements encoding transcriptional regulation and chromatin structure, we improved the fraction of expression variation that was previously shown to be explained based on known cis-transcriptional effects by approximately 3-fold. Taken together, our analysis highlights the importance of chromatin divergence involved in expression evolution between paralogs.

PhosSNP for systematic analysis of genetic polymorphisms that influence protein phosphorylation.

We are entering the era of personalized genomics as breakthroughs in sequencing technology have made it possible to sequence or genotype an individual person in an efficient and accurate manner. Preliminary results from HapMap and other similar projects have revealed the existence of tremendous genetic variations among world populations and among individuals. It is important to delineate the functional implication of such variations, i.e. whether they affect the stability and biochemical properties of proteins. It is also generally believed that the genetic variation is the main cause for different susceptibility to certain diseases or different response to therapeutic treatments. Understanding genetic variation in the context of human diseases thus holds the promise for "personalized medicine." In this work, we carried out a genome-wide analysis of single nucleotide polymorphisms (SNPs) that could potentially influence protein phosphorylation characteristics in human. Here, we defined a phosphorylation-related SNP (phosSNP) as a non-synonymous SNP (nsSNP) that affects the protein phosphorylation status. Using an in-house developed kinase-specific phosphorylation site predictor (GPS 2.0), we computationally detected that approximately 70% of the reported nsSNPs are potential phosSNPs. More interestingly, approximately 74.6% of these potential phosSNPs might also induce changes in protein kinase types in adjacent phosphorylation sites rather than creating or removing phosphorylation sites directly. Taken together, we proposed that a large proportion of the nsSNPs might affect protein phosphorylation characteristics and play important roles in rewiring biological pathways. Finally, all phosSNPs were integrated into the PhosSNP 1.0 database, which was implemented in JAVA 1.5 (J2SE 5.0). The PhosSNP 1.0 database is freely available for academic researchers.