Sympatric Speciation in Mole Rats and Wild Barley and Their Genome Repeatome Evolution: A Commentary

Abstract The theories of sympatric speciation (SS) and coding and noncoding (cd and ncd =repeatome)  genome function are still contentious. Studies on SS in our two new models, “Evolution Canyon” and “Evolution Plateau”, in Israel, divergent microclimatically and geologically‐edaphically, respective...

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Main Authors: Eviatar Nevo, Kexin Li
Format: Article
Language:English
Published: Wiley 2022-12-01
Series:Advanced Genetics
Subjects:
Online Access:https://doi.org/10.1002/ggn2.202200009
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author Eviatar Nevo
Kexin Li
author_facet Eviatar Nevo
Kexin Li
author_sort Eviatar Nevo
collection DOAJ
description Abstract The theories of sympatric speciation (SS) and coding and noncoding (cd and ncd =repeatome)  genome function are still contentious. Studies on SS in our two new models, “Evolution Canyon” and “Evolution Plateau”, in Israel, divergent microclimatically and geologically‐edaphically, respectively, indicated that in ecologically divergent microsites SS is a common speciation model across life from bacteria to mammals. Genomically, the intergenic ncd repeatome was and is still regarded by many biologists as “selfish,” “junk,” and non‐functional. In contrast, it is considered by the encyclopedia of DNA elements discovery as biochemically functional and regulatory, and the transposable elements were considered earlier by Barbara McClintock as “controlling elements” of genes. Remarkably, it is found that repeated elements can statistically identify significantly, the five species of subterranean mole rats of Spalax ehrenbergi superspecies adapted to increasingly arid climatic trend southward in Israel. Moreover, it is first discovered in the SS studies in two distant taxa, subterranean mole rats and wild barley, and later also in spiny mice in Israel and subterranean zokors in China, that the noncoding repeatome is genomically mirroring the image of the protein‐coding genome in divergent ecologies. It is shown that this mirroring image is statistically significant both within and between the ecologically divergent taxa supporting the hypothesis that much of the repeatome might be regulatory and selected as the protein‐coding genome by the same ecological stresses.
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spelling doaj.art-c1b9135af2434d02bd4b9f0886768f562022-12-23T02:32:11ZengWileyAdvanced Genetics2641-65732022-12-0134n/an/a10.1002/ggn2.202200009Sympatric Speciation in Mole Rats and Wild Barley and Their Genome Repeatome Evolution: A CommentaryEviatar Nevo0Kexin Li1Institute of Evolution University of Haifa Haifa 3498838 IsraelState Key Laboratory of Grassland Agro‐ecosystem College of Ecology Lanzhou University Lanzhou 730000 ChinaAbstract The theories of sympatric speciation (SS) and coding and noncoding (cd and ncd =repeatome)  genome function are still contentious. Studies on SS in our two new models, “Evolution Canyon” and “Evolution Plateau”, in Israel, divergent microclimatically and geologically‐edaphically, respectively, indicated that in ecologically divergent microsites SS is a common speciation model across life from bacteria to mammals. Genomically, the intergenic ncd repeatome was and is still regarded by many biologists as “selfish,” “junk,” and non‐functional. In contrast, it is considered by the encyclopedia of DNA elements discovery as biochemically functional and regulatory, and the transposable elements were considered earlier by Barbara McClintock as “controlling elements” of genes. Remarkably, it is found that repeated elements can statistically identify significantly, the five species of subterranean mole rats of Spalax ehrenbergi superspecies adapted to increasingly arid climatic trend southward in Israel. Moreover, it is first discovered in the SS studies in two distant taxa, subterranean mole rats and wild barley, and later also in spiny mice in Israel and subterranean zokors in China, that the noncoding repeatome is genomically mirroring the image of the protein‐coding genome in divergent ecologies. It is shown that this mirroring image is statistically significant both within and between the ecologically divergent taxa supporting the hypothesis that much of the repeatome might be regulatory and selected as the protein‐coding genome by the same ecological stresses.https://doi.org/10.1002/ggn2.202200009“Evolution Canyon”“Evolution Plateau”coding and noncoding genomesgenome mirroringrepeatomesubterranean mole rats
spellingShingle Eviatar Nevo
Kexin Li
Sympatric Speciation in Mole Rats and Wild Barley and Their Genome Repeatome Evolution: A Commentary
Advanced Genetics
“Evolution Canyon”
“Evolution Plateau”
coding and noncoding genomes
genome mirroring
repeatome
subterranean mole rats
title Sympatric Speciation in Mole Rats and Wild Barley and Their Genome Repeatome Evolution: A Commentary
title_full Sympatric Speciation in Mole Rats and Wild Barley and Their Genome Repeatome Evolution: A Commentary
title_fullStr Sympatric Speciation in Mole Rats and Wild Barley and Their Genome Repeatome Evolution: A Commentary
title_full_unstemmed Sympatric Speciation in Mole Rats and Wild Barley and Their Genome Repeatome Evolution: A Commentary
title_short Sympatric Speciation in Mole Rats and Wild Barley and Their Genome Repeatome Evolution: A Commentary
title_sort sympatric speciation in mole rats and wild barley and their genome repeatome evolution a commentary
topic “Evolution Canyon”
“Evolution Plateau”
coding and noncoding genomes
genome mirroring
repeatome
subterranean mole rats
url https://doi.org/10.1002/ggn2.202200009
work_keys_str_mv AT eviatarnevo sympatricspeciationinmoleratsandwildbarleyandtheirgenomerepeatomeevolutionacommentary
AT kexinli sympatricspeciationinmoleratsandwildbarleyandtheirgenomerepeatomeevolutionacommentary