The role of laterally transferred genes in adaptive evolution

Background

Bacterial genomes develop new mechanisms to tide them over the imposing conditions they encounter during the course of their evolution. Acquisition of new genes by lateral gene transfer may be one of the dominant ways of adaptation in bacterial genome evolution. Lateral gene transfer provides the bacterial genome with a new set of genes that help it to explore and adapt to new ecological niches.

Methods

A maximum likelihood analysis was done on the five sequenced corynebacterial genomes to model the rates of gene insertions/deletions at various depths of the phylogeny.

Results

The study shows that most of the laterally acquired genes are transient and the inferred rates of gene movement are higher on the external branches of the phylogeny and decrease as the phylogenetic depth increases. The newly acquired genes are under relaxed selection and evolve faster than their older counterparts. Analysis of some of the functionally characterised LGTs in each species has indicated that they may have a possible adaptive role.

Conclusion

The five Corynebacterial genomes sequenced to date have evolved by acquiring between 8 – 14% of their genomes by LGT and some of these genes may have a role in adaptation.

     

YABBY polarity genes mediate the repression of KNOX homeobox genes in Arabidopsis

The YABBY (YAB) genes specify abaxial cell fate in lateral organs in Arabidopsis. Loss-of-function mutants in two early-expressing YAB genes, FILAMENTOUS FLOWER (FIL) and YAB3, do not exhibit vegetative phenotypes as a result of redundancy. Mutations in these genes result in the derepression of the KNOX homeobox genes SHOOTMERISTEMLESS (STM), BREVIPEDICELLUS, and KNAT2 in the leaves and in the partial rescue of stm mutants. Here, we show that fil yab3 double mutants exhibit ectopic meristem formation on the adaxial surfaces of cotyledons and leaf blades. We propose that in addition to abaxial specification, lateral organ development requires YAB function to downregulate KNOTTED homeobox genes so that meristem initiation and growth are restricted to the apex.     

Leaving the meristem behind: regulation of KNOX genes

The mechanism by which the plant reserves some cells as pluripotent stem cells while partitioning others into differentiated leaf tissue is fundamental to plant development. New work in Arabidopsis elucidates the genetic circuitry that distinguishes meristem from leaf.     

The role of parasites in generating evolutionary novelty

In this review, David Bermudes and Keith Joiner discuss the interrelationship between parasitism and mutualism and examine the parallel mechanisms used by parasites and mutualists to access and persist within the intracellular environment. By drawing analogies with mutualistic associations, they suggest mechanisms by which some parasites may ultimately benefit their hosts. They further speculate that some hosts may even become dependent upon their parasites.     

Homeotic genes and their role in development of wheat's morphological traits

The information concerning major families of plant homeotic genes, ways of their expression regulation and role in plant morphogenesis is outlined. Role of known homeotic genes in wheat development and growth habit establishment is presented. A supposed role of homeotic genes in major morphologic traits formation is discussed.     

The role of marine biota in the evolution of terrestrial biota: Gases and genes

There is greater biodiversity (in the senseof genetic distance among higher taxa) ofextant marine than of terrestrialO₂-evolvers. In addition tocontributing the genes from one group ofalgae (Class Charophyceae, DivisionChlorophyta) to produce by evolution thedominant terrestrial plants (Embryophyta),the early marine O₂-evolvers greatlymodified the atmosphere and hence the landsurface when the early terrestrialO₂-evolvers grew. The earliestterrestrial phototrophs (from geochemicalevidence) occurred 1.2 Ga ago, over 0.7 Gabefore the Embryophyta evolved, but wellafter the earliest marine (cyanobacterial)O₂ evolvers (3.45 Ga) and marineeukaryotic O₂ evolvers (2.1 Ga). Evenby the time of evolution of the earliestterrestrial O₂-evolvers the marineO₂-evolvers had modified the atmosphereand land environment in at least thefollowing five ways. Once photosyntheticO₂ paralleling organic C burial hadsatisfied marine (Fe²⁺, S^2-reductants, atmospheric O₂ built (1) upto a considerable fraction of the extantvalue (although some was consumed inoxidising terrestrial exposed Fe²⁺ and(2) provided stratospheric O₃ and thusa UV-screen. (3) CO₂ drawdown to20-30times the extant level is attributableto net production, and burial, of organic Cin the oceans (plus other geologicalprocesses). Furthermore, (4) theirproduction of volatile organic S compoundscould have helped to supply S to inland sitesbut also (5) delivered Cl and Br to thestratosphere thus lowering the O₃ leveland the extent of UV screening.     

Homeotic genes and their role in development of morphological traits in wheat

Information about main families of plant homeotic genes, ways of their activity regulation, and role in morphogenesis is presented. The role of known homeotic genes in wheat development and possible participation of homeotic genes in the development of main morphological traits of this species is discussed.     

Reduced leaf complexity in tomato wiry mutants suggests a role for PHAN and KNOX genes in generating compound leaves

Recent work on species with simple leaves suggests that the juxtaposition of abaxial (lower) and adaxial (upper) cell fates (dorsiventrality) in leaf primordia is necessary for lamina outgrowth. However, how leaf dorsiventral symmetry affects leaflet formation in species with compound leaves is largely unknown. In four non-allelic dorsiventrality-defective mutants in tomato, wiry, wiry3, wiry4 and wiry6, partial or complete loss of ab-adaxiality was observed in leaves as well as in lateral organs in the flower, and the number of leaflets in leaves was reduced significantly. Morphological analyses and expression patterns of molecular markers for ab-adaxiality [LePHANTASTICA (LePHAN) and LeYABBY B (LeYAB B)] indicated that ab-adaxial cell fates were altered in mutant leaves. Reduction in expression of both LeT6 (a tomato KNOX gene) and LePHAN during post-primordial leaf development was correlated with a reduction in leaflet formation in the wiry mutants. LePHAN expression in LeT6 overexpression mutants suggests that LeT6 is a negative regulator of LePHAN. KNOX expression is known to be correlated with leaflet formation and we show that LeT6 requires LePHAN activity to form leaflets. These phenotypes and gene expression patterns suggest that the abaxial and adaxial domains of leaf primordia are important for leaflet primordia formation, and thus also important for compound leaf development. Furthermore, the regulatory relationship between LePHAN and KNOX genes is different from that proposed for simple-leafed species. We propose that this change in the regulatory relationship between KNOX genes and LePHAN plays a role in compound leaf development and is an important feature that distinguishes simple leaves from compound leaves.     

Coordination of leaf development via regulation of KNOX1 genes

Class I KNOTTED1-LIKE HOMEOBOX (KNOX1) genes are expressed in the shoot apical meristem (SAM) to effect its formation and maintenance. KNOX1 genes are also involved in leaf shape control throughout angiosperm evolution. Leaves can be classified as either simple or compound, and KNOX1 expression patterns in leaf primordia are highly correlated with leaf shape; in most simple-leafed species, KNOX1 genes are expressed only in the SAM but not in leaf primordia, while in compound-leafed species they are expressed both in the SAM and leaf primordia. How can KNOX1 expression be maintained to a high degree in the SAM, but simultaneously be so variable in leaves? This dichotomy suggests that the processes of leaf and SAM development have been compartmentalized during evolution. Here, we introduce our findings regarding the regulation of expression of SHOOT MERISTEMLESS, a KNOX1 gene, together with a brief review of KNOX1 genes from an evolutionary viewpoint. We also present our findings regarding another aspect of KNOX1 regulation via a protein–protein interaction network involved in the natural variation in leaf shape. Both aspects of KNOX1 regulation could be utilized for fine-tuning leaf morphology during evolution without affecting the essential function of KNOX genes in the shoot.     

The genetics of plant morphological evolution.

Considerable progress has been made in identifying genes that are involved in the evolution of plant morphologies. Elements of the ABC model of flower development are conserved throughout angiosperms, and homologous MADS-box genes function in gymnosperm reproduction. Candidate gene and mapping analyses of floral symmetry, sex determination, inflorescence architecture, and compound leaves provide intriguing glimpses into the evolution of morphological adaptations.     

Meiosis genes in Daphnia pulex and the role of parthenogenesis in genome evolution

Background  

Thousands of parthenogenetic animal species have been described and cytogenetic manifestations of this reproductive mode are well known. However, little is understood about the molecular determinants of parthenogenesis. The Daphnia pulex genome must contain the molecular machinery for different reproductive modes: sexual (both male and female meiosis) and parthenogenetic (which is either cyclical or obligate). This feature makes D. pulex an ideal model to investigate the genetic basis of parthenogenesis and its consequences for gene and genome evolution. Here we describe the inventory of meiotic genes and their expression patterns during meiotic and parthenogenetic reproduction to help address whether parthenogenesis uses existing meiotic and mitotic machinery, or whether novel processes may be involved.