2016年2月18日 星期四

Hemoglobins and Hb related genes

雖然是很早就知道,也很早就有人研究,不過,還是重新瞭解一下吧。

Evolution of hemoglobin and its genes

by Hardison RC


Abstract
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Insights into the evolution of hemoglobins and their genes are an abundant source of ideas regarding hemoglobin function and regulation of globin gene expression. This article presents the multiple genes and gene families encoding human globins, summarizes major events in the evolution of the hemoglobin gene clusters, and discusses how these studies provide insights into regulation of globin genes. Although the genes in and around the α-like globin gene complex are relatively stable, the β-like globin gene clusters are more dynamic, showing evidence of transposition to a new locus and frequent lineage-specific expansions and deletions. The cis-regulatory modules controlling levels and timing of gene expression are a mix of conserved and lineage-specific DNA, perhaps reflecting evolutionary constraint on core regulatory functions shared broadly in mammals and adaptive fine-tuning in different orders of mammals.
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深入探究血紅蛋白(hemoglobins)與其基因的演化,提供我們對血紅蛋白的功能與基因表現調節的豐富題材。本論文主要針對幾種人類 globin 基因與基因家族,歸納血紅蛋白基因簇演化過程中的主要歷程,並討論這些研究如何深入闡明血紅蛋白的調節。座落於 alpha-like globin 基因複合集(α-like globin gene complex)內或周圍的基因相對地比較穩定,而beta-like globin 則有較大的變動,這可能是基因移動到一個新位置的證據,以及常見的族系專有(lineage-specific)的增多或刪減。控制基因表現量與表現時機的順位調節模組(cis-regulatory module)是保守性的與族系特有的DNA 綜合效果,這或許能反映出哺乳類廣泛共有的核心調控功能的演化限制,以及哺乳綱不同目別物種的適應性微調。

What is Hemoglobin ?

  • transport/bind oxygen
  • it is an abundant proteins in red blood cells of mammals and other jawed vertebrates (gnathostomes). 
  • In human, Hb is known as a heterotetramer : two α-globin and two β-globin, each with an associated heme group.


The model of evolution of vertebrate globin genes. Figure 1 of this reference.
  • Myoglobin:  monomeric heme-bound globin protein found predominantly in skeletal and heart muscle.  It has long been described as an oxygen storage protein.
  • Cytoglobin: found in many tissues.
  • neuroglobin: Its mRNA is abundant in brain tissue but also is present in many other tissues. It is related to invertebrate nerve globins.
  • Physiological function of the heme-bearing proteins are "oxygen binding".  But, CYGB showing nitric oxide dioxygenase activity (converting NO to NO3-) and NGB showing nitrite reductase activity to form nitric oxide  (converting NO3- to NO. This catalytic capability also found in MB and deoxy-Hb). Thus, the nitrite reductase activity could provide a means to produce nitric oxide under hypoxic conditions, signaling from which could regulate mitochondrial respiration and protect tissues (nerves by NGB, heart muscle by MB) from damage under ischemic conditions (Dietz 2011). 
  • MB, CYGB, and NGB are present as single-copy genes, whereas HBB and HBAs are in clusters with multiple related genes.
  • cyclostomes (represented by hagfish and lampreys), also use a heme-containing globin for oxygen transport, but surprisingly, it is more closely related to CYGB than to the gnathostome hemoglobins. This suggests that the oxygen transport function of heme-containing globins arose by independent, convergent evolution in the two major branches of vertebrates. (((Is there sure, solid evidences for these conclusions, or just speculation by the authors?)))
  • Human: alpha-, beta-, delta-, tau-, epsilon- globin.  expressed in different locations / different dev stage. The hemoglobins produced at distinct developmental stages have different affinities for oxygen and are subject to complex regulation by cofactors, favoring an overall movement of oxygen from the maternal bloodstream to that of the fetus or embryo.
  • In human, the separation of α-like and β-like globin gene clusters in amniotes requires coordination of expression between different chromosomes. 人類 (有羊膜類)的α-like and β-like globin gene clusters 分別在不同的染色體,需要協同控制表現。
  • Fish species show an interesting contrast, in that the gene cluster orthologous (homologous genes generated by a speciation event) to that of the mammalian α-globin gene cluster contains both α-like and β-like globin genes ((((((the expression level is not like to be in this guess))))))))) 魚類的 α 與 β globins 則在同一個 cluster 中 (MN type) 
    • MN: found in all gnathostomes being examined. flanked on one side by the genes MPGNPRL3
    • LA (or LCA):  The globin genes in this locus are flanked by the genes LCMT1 and AQP8, and the locus can be called “LA.” The gene ARHGAP17 is also part of this locus in many species. These three nonglobin genes are in the same arrangement and order in the tetrapods (human, platypus, chicken, and frog), but the globin genes is devoid
    • DS: DCHS1 on one side and STIM1 on the other; the RRM1 gene is adjacent to STIM1 in many species. In placental mammals, hundreds of OR genes are in this locus, with additional multigene families such as TRIM genes. (DCHS1 and STIM1 are spanned by many many genes==>several megabases away). Found in "amniotes" (water-tighted environment for embryo. reptiles, birds, mammals) but absent in fish and amphibians.
      b-like globin only.  


Models for evolution of hemoglobin gene complexes in jawed vertebrates. Figure 2 from the reference. The gene maps are not complete, nor are they to scale. (This diagram is adapted fromHardison 2008.)





Maps of orthologous α-like globin genes and expression timing in amniotes. Figure 2 from the reference. 

The history of the gene clusters encoding hemoglobins is dynamic and complex.  (((inferred to be a more adaptive to the environment).

The ortholog of the μ-globin gene is expressed in adult erythroid cells in birds, producing αD-globin

Hemoglobin gene expression is restricted to erythroid cells.

===================... contents in the further section discuss the gene regulation, gene origins, ...... are majorly in "mammal", not my interesting subject now.  so I skipped   


2016年2月16日 星期二

choanoglafellate

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另一個題外話: choanoglafellate  (wiki : https://en.wikipedia.org/wiki/Choanoflagellate),  a group of free-living unicellular and colonial flagellate eukaryotes considered to be the closest living relatives of the animals.

The cell body of many choanoflagellates is surrounded by a distinguishing extracellular matrix or periplast.

A free living SPERM ? with a Coat/ a reinforced, moving home?


The choanoflagellates feed on bacteria. Movement of the flagellum draws water through the collar, and bacteria and detritus are captured by the microvilli and ingested.Water currents generated by the flagellum also push free-swimming cells along, as in animal sperm.


A model of S. rosetta life history. Fig 2 from "Cell differentiation and morphogenesis in the colony-forming choanoflagellate Salpingoeca rosetta" by Dayel et al., 2011. (doi:10.1016/j.ydbio.2011.06.003


Analysis on molecular phylogenetic analysis on SSU, LSU, a-tubulin and hsp90 found that choanoflagellates are strongly supported as monophyletic and confirm their position as the closest known unicellular living relative of animals.

Two choanoflagellate species have had their genomes fully sequenced, with another two species having had transcriptome data published.






Previously, Choanoflagellida was divided into these three families based on the composition and structure of their periplast; now with classification based on molecular phylogenetics.  The choanocytes (also known as "collared cells") of sponges (considered among the most basal metazoa) have the same basic structure as choanoflagellates. Collared cells are found in other animal groups, such as ribbon worms,[17] suggesting this was the morphology of their last common ancestor.




The SIT gene family shows little or no homology to any other genes, even to genes in non-siliceous choanoflagellates or stramenopiles. This suggests that the SIT gene family evolved via a lateral gene transfer event between Acanthoecids and Stramenopiles.


Broad Institute Project:
Origins of Multicellularity Database

The Origins of Multicellularity Project was funded by the NHGRI and is described in a white paper and a recent publication.


2016年2月15日 星期一

Trichoplax adhaerens

Today I learn a species/ a clade that is thought to be the most primitive metazoan form.


Greek “tricha" = ‘hair’ and “plax" = ‘plate’, Latin “adhaerere" = ‘to stick’




Figure 1 from "Chasing the urmetazoon: Striking a blow for quality data?" by Osigus et al,, 2013 ( doi:10.1016/j.ympev.2012.05.028) (A) Photograph of Trichoplax adhaerens, Schulze (1883). For additional images of placozoan specimens see www.trichoplax.com. (B) Modern placula hypothesis of metazoan origin (for details see Schierwater et al., 2009a). (from Schierwater et al., 2009a).

And the phylogenetic location of this clade:


Maximum likelihood phylogenetic tree of metazoan relationships using a concatenated data matrix. Figure 3 from "Global Diversity of the Placozoa" by Eitel et al., 2013 (doi: 10.1371/journal.pone.0057131)



The body is in this structure:


Revised schematic cross sections of a Placozoon.  Figure 2 from "Global Diversity of the Placozoa" by Eitel et al., 2013 (doi: 10.1371/journal.pone.0057131)


And total ~10 types of cells are identified. 

Trichoplax has a small genome (smallest metazoan genome?) in comparison to other animals, nearly 87% of its 11,514 predicted protein-coding genes are identifiably similar to known genes in other animals.

wiki https://en.wikipedia.org/wiki/Trichoplax

Some interesting references:

Trichoplax adhaerens
Representative genome: Trichoplax adhaerens (assembly v1.0)
Download sequences in FASTA format for genome, transcript, protein
Download genome annotation in GFF, GenBank or tabular format
BLAST against Trichoplax adhaerens genome, transcript, protein 

T. Driscoll, J. J. Gillespie, E. K. Nordberg, A. F. Azad, B. W. Sobral, Bacterial DNA Sifted from the Trichoplax adhaerens (Animalia: Placozoa) Genome Project Reveals a Putative Rickettsial Endosymbiont, Genome Biology and Evolution, 2013, 5, 4, 621CrossRef

Tracing the published BioProject of Placozoa, I found this paper:


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Digest from  the 8x assembly manuscript

The Trichoplax genome and the nature of placozoans

by Srivastava M et al., 2008. Nature 454, 955-960 (21 August 2008) | doi:10.1038/nature07191; 


[Backgrounds]

  • Ecological Location:
    throughout tropical and subtropical oceans in nearshore habitats, particularly mangrove communities
  • Classifications and Nomenclature:
    The only named species in the phylum is Trichoplax adhaerens, while the morphologically indistinguished individuals from various locations shows great divergency in DNA level, suggesting cryptic species may exist.
  • Body Structure:
    a flat disc of cells consisting of two epithelial layers, which sandwich a layer of multinucleate fibre cells. Only four cell types have been described previously. Nerves, sensory cells and muscle cells are apparently absent. 
    No evident body axes other than top versus bottom and periphery versus interior are defined. They show no regular directionality in their movement.
  • Known Behaviors:
    • Moving:
      the animals move by cilia on the bottom surface and by the fibre cell layer. 
    • Feeding:
      Trichoplax climbs atop its food using the bottom surface as a temporary extraorganismal gastric cavity; digestion is both extracellular and phagocytic.
    • Breeding:
      In culture, Trichoplax reproduces by fission, whereby two (sometimes three) parts of the animal move away from each other until their connection is ruptured.
      Sexual reproduction is suggested but has not been observed.  Putative oocyte formation in degenerating animals is routinely seen. These large cells have been observed to undergo cleavage up to a 256-cell stage before degenerating (unpublished observations). Sperm have been described once without other investigators proofs. Population genetic analyses, however, demonstrate allelic variation and evidence for genetic recombination in animals in the wild that is consistent with sex.
[genome]

  • karyotype study (from another paper: On the Karyotype of Trichoplax sp. by Birstein, V.J 1989 )
    • 2n=12.  3 pairs of bi-armed (meta- or submetacentrics) and 3 pairs of acrocentrics.
    • dorsal / ventral layers are in 2n; intermediate are possibly tetraploid.
    • Comparing to other primitive metazoans:
      ** Turbellaria (渦蟲): 2n=10~20, C ~0.4 to 1.2 pg. and often bi-armed.
      ** Sponges and polyp (Cnideria) C = 0.5~0.6 pg, 10x to Trichoplax. Other Cnideria shows even larger C value.  Chromosome number of sponges may be double to Trichoplax (2n=24) or even in polyploid way (4n ~44 or 6n ~66)
    • The genome size and chromosome number are comparable to Protozoans.
    • ** Karyotypes of sp in Protomonadida, Polymastigida are in 6~10.
      ** some parasitic flagellates (Trypanosoma, Leishmania) are in 0.1~0.2pg/nucleus (2n ?)
  • Nucleus genome
    The genome size was estimated at 0.08 pg/haploid genome using Feulgen staining.

    Because there are at present no genetic or physical maps of Trichoplax, we could not reconstruct entire chromosomes, but the completeness of the draft assembly (98% of the 14,571 expressed sequence tags (ESTs) align) and its long-range linkage (19 scaffolds longer than 1 Mb represent 80% of the assembly) make it an excellent substrate for annotation and comparative analysis (Supplementary Information).

    source: The "Grell" strain, a single clonal lineage kept from 1969. Animals were grown on a monoculture of the cryptophyte alga Pyrenomonas helgolandii. 12,000 individual Trichoplax specimens were picked by hand, washed individually and subjected to DNA extraction using a standard protocol

  • Mitochondria (reported previously)





















An estimated 8 million metazoan species currently inhabit the Earth's aquatic and terrestrial environments, a predicted 86% of which have not been characterized (Mora, Tittensor, Adl, Simpson, & Worm, 2011).