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ICRISAT Archival Report 2006 - The seedlings of success in the ...

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<strong>The</strong> phenotyp<strong>in</strong>g <strong>of</strong> F 6 <strong>in</strong>bred progenies <strong>of</strong> <strong>the</strong> mapp<strong>in</strong>g population developed between 841B (tolerant) and 863B<br />

(sensitive) has been <strong>in</strong>itiated and <strong>the</strong> harvest<strong>in</strong>g is underway.<br />

V<strong>in</strong>cent Vadez and CT Hash<br />

Milestone 5B.2.1.2: Putative QTLs for sal<strong>in</strong>ity tolerance based on 35 BC 6 F 3 contiguous segment <strong>in</strong>trogression<br />

l<strong>in</strong>es identified (CTH/SS/VV, 2010)<br />

Fund<strong>in</strong>g to complete development <strong>of</strong> <strong>the</strong> contiguous segment <strong>in</strong>trogression l<strong>in</strong>e set, and <strong>in</strong>itiate its assessment, was<br />

received from DBT <strong>in</strong> December <strong>2006</strong>, so work towards this milestone on this will recommence <strong>in</strong> 2007.<br />

Milestone 5B.2.1.3: New F 6 RIL mapp<strong>in</strong>g populations for sal<strong>in</strong>ity tolerance available <strong>in</strong> pearl millet for<br />

phenotyp<strong>in</strong>g and genotyp<strong>in</strong>g (CTH/BVSR/KNR/VV, 2009)<br />

<strong>The</strong> exist<strong>in</strong>g (ICMB 841-P3 x 863B-P2)-derived pearl millet mapp<strong>in</strong>g population was advanced to F6 RILs. <strong>The</strong><br />

new RILs are be<strong>in</strong>g skeleton mapped as part <strong>of</strong> an exercise to create a more <strong>in</strong>formative pearl millet consensus<br />

l<strong>in</strong>kage map. Seed <strong>of</strong> approximately 150 progenies <strong>of</strong> this RIL mapp<strong>in</strong>g population are now available for sal<strong>in</strong>ity<br />

tolerance screen<strong>in</strong>g while new pearl millet RIL mapp<strong>in</strong>g populations are be<strong>in</strong>g generated for this target trait. Crosses<br />

were made between several selected pairs <strong>of</strong> sorghum parental l<strong>in</strong>es exhibit<strong>in</strong>g substantial pair-wise dissimilarity<br />

(>70%) at 67 SSR loci distributed across all 10 sorghum l<strong>in</strong>kage groups, as well as substantial phenotypic<br />

differences for sal<strong>in</strong>ity tolerance based on pot screens <strong>of</strong> 30 candidate parental l<strong>in</strong>es. F1 hybrids from several such<br />

crosses were sown for advance to <strong>the</strong> F2 generation by self<strong>in</strong>g dur<strong>in</strong>g <strong>the</strong> <strong>2006</strong>/07 postra<strong>in</strong>y season.<br />

Output target 5B.3: Breed<strong>in</strong>g value <strong>of</strong> putative term<strong>in</strong>al drought tolerance QTLs <strong>in</strong> pearl millet documented<br />

(2009)<br />

Activity 5B.3.1: Publication <strong>of</strong> earlier results on drought tolerance QTL and gene pyramid<strong>in</strong>g<br />

Milestone 5B.3.1.1: Publication <strong>of</strong> results from marker-assisted selection for <strong>the</strong> l<strong>in</strong>kage group 2 drought<br />

tolerance QTL <strong>in</strong>to <strong>the</strong> genetic background <strong>of</strong> two parental l<strong>in</strong>es (CTH/FRB, 2008)<br />

QTL for improved gra<strong>in</strong> yield across variable gra<strong>in</strong>-fill<strong>in</strong>g moisture environments: Previous molecular work<br />

on drought tolerance <strong>in</strong> pearl millet has focused on QTL for <strong>the</strong> ability to ma<strong>in</strong>ta<strong>in</strong> yield under post-flower<strong>in</strong>g<br />

drought stress, which can be easily transferred to o<strong>the</strong>rwise well-adapted hybrid parents to improve <strong>the</strong> performance<br />

<strong>of</strong> <strong>the</strong>ir hybrids under this type <strong>of</strong> stress. Pearl millet breed<strong>in</strong>g programs target<strong>in</strong>g adaptation to variable postflower<strong>in</strong>g<br />

moisture environments would benefit from QTLs that improve gra<strong>in</strong> yield across <strong>the</strong> full range <strong>of</strong> postflower<strong>in</strong>g<br />

moisture conditions, ra<strong>the</strong>r than <strong>in</strong> just some specific drought-stressed environments. We reanalyzed an<br />

extensive (12 environment) phenotyp<strong>in</strong>g data set that <strong>in</strong>cluded both stressed and non-stressed post-flower<strong>in</strong>g<br />

environments, to identify QTLs for improved yield over <strong>the</strong> whole range <strong>of</strong> moisture environments. Genetic<br />

materials were testcrosses <strong>of</strong> 79 F 2 -derived F 4 progenies from a mapp<strong>in</strong>g population based on a widely adapted<br />

ma<strong>in</strong>ta<strong>in</strong>er l<strong>in</strong>e (ICMB 841) × a post-flower<strong>in</strong>g drought tolerant ma<strong>in</strong>ta<strong>in</strong>er (863B). Three QTLs (on LG 2, LG 3,<br />

LG 4) were identified as primary candidates for MAS for improved gra<strong>in</strong> yield across variable post-flower<strong>in</strong>g<br />

moisture environments. QTLs on LG 2 and LG 3 (<strong>the</strong> most promis<strong>in</strong>g) expla<strong>in</strong>ed a useful proportion (13 to 25%) <strong>of</strong><br />

phenotypic variance for gra<strong>in</strong> yield across environments. <strong>The</strong>y also co-mapped with QTLs for harvest <strong>in</strong>dex across<br />

environments, and with QTLs for both gra<strong>in</strong> number and <strong>in</strong>dividual gra<strong>in</strong> mass under severe term<strong>in</strong>al stress. Nei<strong>the</strong>r<br />

had a significant QTL × environment <strong>in</strong>teraction, <strong>in</strong>dicat<strong>in</strong>g <strong>the</strong>ir predicted effects should occur across a broad range<br />

<strong>of</strong> available moisture environments. F<strong>in</strong>ally, both are l<strong>in</strong>ked to SSR markers so <strong>the</strong>y are amenable to efficient MAS.<br />

<strong>The</strong> rema<strong>in</strong><strong>in</strong>g QTL (LG 4) is <strong>of</strong> secondary <strong>in</strong>terest as it has a less consistent performance across <strong>in</strong>dividual<br />

moisture environments and a less clear effect on secondary traits. Responses to MAS predicted for each <strong>of</strong> <strong>the</strong><br />

identified gra<strong>in</strong> yield QTLs ranged from 70 to 100 kg ha -1 across environments and as much 160 kg ha -1 <strong>in</strong><br />

<strong>in</strong>dividual moisture environments.<br />

FR Bid<strong>in</strong>ger, T Nepoleon and CT Hash<br />

Improvement <strong>of</strong> <strong>the</strong> post-flower<strong>in</strong>g drought tolerance <strong>of</strong> ICMB 841 by MABC: We completed <strong>the</strong> evaluation <strong>of</strong><br />

13 BC 5 F 3 segmental <strong>in</strong>trogression l<strong>in</strong>es target<strong>in</strong>g <strong>the</strong> LG 2 QTL (for post-flower<strong>in</strong>g drought tolerance) from 863B <strong>in</strong><br />

<strong>the</strong> background <strong>of</strong> widely adapted seed parent ICMB 841. <strong>The</strong>se segmentally near-isogenic l<strong>in</strong>es were evaluated <strong>in</strong><br />

testcross hybrid form (with both drought-tolerant and drought-susceptible testers) <strong>in</strong> multiple years <strong>in</strong> both <strong>the</strong><br />

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